<?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>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>1989</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Photochemical Rearrangement of 8- methyl
Spiro [2.5] oct-7-en-4-one to 4-methyl
Spiro [2.5] oct-4-en-6-one</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31170</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>Irradiation of &amp;methyl spiro [2.5] oct-7-en-4-one through its singlet excited
state resulted in the formation of 4-methyl spirO [2.5]  oct-4-en -6-one. We have
used the cyclopropyl moiety in the molecule as a probe to study the operating
mechanism in the photochemistry of ?, ?-unsaturated compounds. The results
showed that this photoisomerization probably occurs through a concerted
process.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31170_93a819cbd635bd1505ef0f804c21cc2a.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
