<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>THE EFFECT OF SULFUR MUSTARD ON
GLUCOSE PHOSPHORYLATING ENZYMES
AND LIVER CELLS IN MALE RATS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31220</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>A significant decrease of hepatic high-Km glucose- phosphorylating enzyme
glucokinase (ATP- D- glucose 6- phosphotransferase, EC 2.7. 1.2, GK) and low-Km
hexokinases (EC 2.7. 1.1. HK) activities were noticed in liver treated with 2, 2&#039;-
dichlorodiethyl sulfide (sulfur mustard, HD) when injectedinteraperitoneally to male
rats in 114 LD50. This decrease occurred 1.5  to 5.5 hours after the injection.
Simultaneously, a significant decrease in concentration of soluble protein and
glycogen was also noted after2 hours. In addition some morphological changes on liver
cells were noticed</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31220_398fe2ec0161a64eb0ce33ece464fc06.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>THE INHIBITORY EFFECT OF DEHYDROEPIANDROSTERONE
ON THE ACTIVITY
AND ISOENZYME PATTERNS OF LIVER GLUCOSE
6-PHOSPHATE DEHYDROGENASE
DURING DIFFERENT STAGES OF GROWTH</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31221</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The effect of dehydroepiandrosterone (DHEA) on the activity and isoenzyme
patterns of liver glucose 6- phosphate dehydrogenase (G6PD) was investigated in rats
during different stages of growth. G6PD activity of mature rats was less than those of
the immature (43%) and newborn (35%) animals. DHEA at 10 M) inhibited G6PD
activity of the mature , immature and newborn rats by 79%, 39% , and 88% ,
respectively. Digitonin (0.02%) abolished the inhibitory effect of DHEA in all three
groups of rats with an additional22% increase in the enzyme activity in only the mature
animals. Gel electrophoresis band patterns of G6PD showed four active bands (I, 11,
111, IV) for the newborn and immature rats. In mature rats band IV was absent but
appeared in the presence of digitonin. When electrophoresis was done in the presence
of DHEA (10  M) band IV of the immature and neivborn animals disappeared and the
activity of band Ifor all animals was partially inhibited with no change in the activities of
bands II and III. The data provide further evidence for the possible regulatory role of
DHEA on G6PD isoenzyme activities</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31221_a6101db109c4529f60805430ce177318.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>THE RELATIONSHIP BETWEEN ALUMINIUM
TOXICITY
AND IRON METABOLISM IN RATS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31222</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The relationship between aluminium toxicity and iron metabolism was studied.
Male rats were exposed to aluminium by daily intraperitoneal injection of 40pmolelkg
body weight. After 45 days, aluminium intoxified rats had a significant loweredserum
ferritin (55%), iron (42%), TIBC (25%) and hemoglobin(31%). At thesame time the
serum ceruloplasmin level was elevated by 60%. This result shows that aluminium
interferes with the iron metabolism in rats and might be considered as a possiblecause
of hypochromic microcytic anemia which is found following regular hemodialysis in
chronic renal failure patients</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31222_d66e6fd222e1c0f49746452faa415c1c.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>EXTRACTIVE SPECTROPHOTOMETRIC
DETERMINATION OF VANADIUM
WITH ANTHRANILIC ACID IN PRESENCE
OF PYRIDINE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31223</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Vanadium (III) gives a greenish- yellow complex with anthranilic acid in presence of
pyridine. The complex is extractable with chloroform and is used for photometric
determination of vanadium by measuring the absorbance at 390 nm against a reagent
blank. Beer&#039;s Law holds good in the range of 1-20 pg V/ml. Moderate amounts of Pb
(II) , Ca (II) , Sr (II) , Ba (II) , Cd (II) , Mg (II) , Mn (II) , Ni (II) , Co (II) , Cu (II) , Zn (II) and limited amounts of W (VI), A1 (III), Th (IV), Zr (IV), Sn (II), Sb (III), Ti(IV), Fe (III), and Cr (VI) can be tolerated. U (VI) and Mo (VI) interfere</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31223_3e1e19f4445b3d8bf303f4771e6973e6.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>LEWIS-BASE ADDUCTS OF LEAD (11) COMPLEXES.
CRYSTAL STRUCTURES OF Pb (BIPY) (H O)
(N0 )  AND Pb (PHEN) (H 0) (NO )</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31224</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Reactions of equemolar amounts of lead (II) nitrate and 2,2&#039;- bipyridine o r l , 10-
phenanthroline in aqueous methanolicsolution yield crystals of Pb (bipy)(H O)(NO )  
(1) or Pb (phen) (H O) (NO )   (2) respectively. Their structures were determined by
X-ray crystallography. The method and structure determination is described</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31224_1b4a70ea8ec6487a12030c6dbde8e3d3.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>PREPARATION AND CHARACTERIZATION
OF Mn (III) COMPLEXES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31225</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>We have prepared and characterized a few Mn (III) complexes by using a few
bidentate and tridentate ligands. Spectra of the manganese (III) ion in a variety of
molecular environments are reported. On the basis of solution spectra, some of these
complexes seem to be typically distorted</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31225_42abbf1997bbf1bea463690de3451e39.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>PHOTOCHEMICAL DECOMPOSITION OF
3-CHLORO-CROTON ALDEHYDE
TOSYLHYDRAZONE SODIUM SALT</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31226</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The low temperature photochemical decomposition of 3- chloro-croton aldehyde
tosylhydrazone sodium salt in tetrahydrofuran results in the formation of 3- chloro- 3-
methyl cyclopropene and 5- chloro- 5- methyl- pyrazolenine respectively. In the
presence of moisture, the photohydrated compound 3 was obtained as one of the
products</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31226_9ffeb5b764e884cc28fef0104e64b5bc.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>2-DIMETHYLPHOSPHONO-(3-METHOXYCAR- B
ONYL) -6- PHENYLACETAMIDO CARBAPENAM</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31227</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The title compound has been synthesized starting from cis- N- (a -
methylacrylyl) -3-N- Phenylacetamido -4- styryl -2- azetidinone (1) [1].</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31227_047213fe37bcee03c915839cffd2024b.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>ATTEMPTED SYNTHESIS OF 5&#039; - DEOXY - 5&#039; -
PHOSPHONO - ISOCYTIDINE
SYNTHESIS OF PHOSPHONIC ACID DERIVATIVES
OF ACYCLO - NUCLEOSIDES. PREPARATION
OF 1- ?- D- ARABINOFURANOSYL
PYRIMIDINES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31228</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The synthesis of 5&#039; - deoxynucleoside 5&#039; - phosphonates which contains a 5&#039; - CP
bond in place of the 5&#039; -COP bond of the naturally occuring nucleotides is described.
The preparation of phosphonate derivatives of acyclo - nucleosides and a simple
method for the conversion of 1-? -D-ribofuranosyl pyrimidines to the corresponding
1-? -D-arabinofuranosyl pyrimidines are also explained</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31228_e5654b80531b9a7338900193f90fbba5.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESIS OF OXAZOLO [3, 2-b] 1, 2, 4-
TRIAZINES
A NOVEL HETEROCYCLIC SYSTEM</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31229</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The synthesis of 6- methyl- 2- phenyl- 7H- oxazolo [3,2-b] 1,2,4-Triazine- 7-one (6,
R=Ph) and its 2-P- bromophenyl analogue to the two members of a new heterocyclic
system is described</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31229_c5cc5960420a4189fb225dbaec8f9e62.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>DEHYDROPUNTARENINE AND
DEHYDROSAULATINE
TO NEW ISOQUINOLINE ALKALOIDS FROM
ROOTS OF BERBERIS ACTINACANTHA</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31230</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The isolation and characterization of two new isoquinoline alkaloids, Dehydropuntarenine
and Dehydrosaulatine, obtained during the column chromatography of an
alkaloidal fraction from the roots of B. Actinacantha (Berberidaceae) are described.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31230_8ebef38fe0b242f7c7a87e7f5b2de305.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESIS OF NEW PHASE- 1 METABOLITES
OF TWO BARBITURATES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31231</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The new 4&#039;- hydroxy and 3&#039;- aldehyde phase- 1 metabolites of butobarbitone and
pentobarbitone are fully synthesized for the first time. These metabolites were used to
idenfity and quantify the natural metabolites in human urine after single and multiple
doses of these drugs. The synthesized metobolites have spectral characterizations (IR,
NMR, U.V. and mass spectroscopy) consisted with the assigned structures</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31231_f80f574e584495515259692b741b890e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>QUINALDINIUM AND POLY(2- VINYLQUINOLINIUM)
DICHROMATES
AS NEW MONOMERIC AND POLYMERIC
OXIDIZING REAGENTS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31232</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Preparation and uses of quinaldinium dichromate and its polymeric analogue poly
(2- vinylquinolinium) dichromate as the new monomeric and polymeric
oxochromium-amine complex reagents for oxidizing variousorganic compounds, with
emphasis on the latter, are described</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31232_2d1838bd5b731e64a54439dac82b3a4e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>KINETIC STUDIES USING SEMI-EMPIRICAL
SELF- CONSISTENT FIELD (SCF) MOLECULAR
ORBITAL (MO) METHOD: PARTI. A MODIFIED
NEGLECT OF DIATOMIC OVERLAP (MNDO)
STUDY OF THE PYROLYSIS OF ETHYL VINYL
ETHER</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31233</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Using a computer code called MOPAC, an acronym for a general Molecular Orbital
Package (Quantum Chemistry Programme Exchange (QCPE) Programme No. 455),
the geometries and heats of formation of the reactant, the products and the trdnsition
state were computed by the MNDO semi- empiricalself consistent field (SCF) method
for the pyrolysis of ethyl vinyl ether. ((Force))calculation on the reactant and the
transition state also gave the enthalpies and entropies at various selected temperatures.
In the temperature range of the experimental pyrolytic study, the above
calculations yielded the Arrhenius parameters of the reaction in excellent agreement
with reported experimental results. This is significant in that it supplements the
number of instances [I, 2,3(a)- (g)], not exhaustively enumerated here, in which a
semi- empirical SCF method has been successfully used to study the reaction
mechanisms of many- atom molecules</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31233_4fac9d25fadd0be196f95f166fec2807.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>KINETIC STUDIES USING SEMI-EMPIRICAL
SELF- CONSISTENT FIELD (SCF) MOLECULAR
ORBITAL (MO) METHOD: PART I1 [I] A
MODIFIED NEGLECT OFDIATOMIC OVERLAP
(MNDO) STUDY OF THE PYROLYSES OF
CHLOROETHYL VINYL ETHERS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31234</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The effect of monochloro and dichloro substitution into the ethyl portion on the
pyrolysis of ethyl vinyl ether has been studied. This involved four possible monosubstituted
derivatives and six disubstituted derivatives. For the monochloro
derivatives, B- chloro substitution enhanced the rate constant while a- chloro
substitution depressed it noticeably. For the dichloro derivatives, substitution of both
chlorine atoms on the same carbon atom, whether aor S hardly made any difference,
while for substitution on different carbon atoms, substrate resulting in transdichloroetbene is facilitated relative to that resulting in the cis product. These results
are interpreted in terms of the effect of the substituent(s) on the electronic charge
density distributions over the key atoms in transition state geometries calculated.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31234_88d619ad97413b44d6659073b7b12f32.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A SUPER ZERO-REST-MASS-EQUATION</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31235</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Various authors have considered the Zero-rest-mass equation and the contour
integral representation of its solutions. Ferber generalized these equations to
supertwistor spaces with 2N odd components so that with N=O we get the standard
ungraded twistors of Penrose. In this paper we use the Batchelor theorem toconstruct
the natural super Twistor space with coarse topology with underlying standard
twistors. We also introduce a Super zero rest-mass equation (S. Z. R. M) which satifies
the standard non- graded Z. R. M. equation when an augmentation map &amp;is applied. It
has been shown that the contour integral defined by Rogers can be used to represent a
solution for these equations and these solutionsreduce to standard solutions when one
applies the ?-map</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31235_d70f195edbc052d647a288e3d46b3b2e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>1</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Additions and Corrections
&quot;M.H.Alamatsaz- On Modality and Divisibility of Poisson
and Binomial Mixtures. J.Sci. I.R. Iran, Vol.l,No.3,
Spring 1990</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31236</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract></Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31236_07c3f887cc69caf06f342a367cfe6304.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
