High yield photolytic reduction of a series of thiaphosphoranes Z p SR to give Z p H
with UV-light-induced tri-n-butyltin hydride through phosphoranyl radical Z p is
described. This reaction is inhibited by a-methylstyrene and initiated by a radical
initiator such as azobisisobutyronitrile
. (1993). EFFICIENT PHOSPHOROUS-SULFUR
BOND REDUCTION IN BICYCLIC
THIAPHOSPHORANES WITH
TRI-n-BUTYLTIN HYDRIDE. (e31155). Journal of Sciences, Islamic Republic of Iran, 4(1), e31155
MLA
. "EFFICIENT PHOSPHOROUS-SULFUR
BOND REDUCTION IN BICYCLIC
THIAPHOSPHORANES WITH
TRI-n-BUTYLTIN HYDRIDE" .e31155 , Journal of Sciences, Islamic Republic of Iran, 4, 1, 1993, e31155.
HARVARD
. (1993). 'EFFICIENT PHOSPHOROUS-SULFUR
BOND REDUCTION IN BICYCLIC
THIAPHOSPHORANES WITH
TRI-n-BUTYLTIN HYDRIDE', Journal of Sciences, Islamic Republic of Iran, 4(1), e31155.
CHICAGO
, "EFFICIENT PHOSPHOROUS-SULFUR
BOND REDUCTION IN BICYCLIC
THIAPHOSPHORANES WITH
TRI-n-BUTYLTIN HYDRIDE," Journal of Sciences, Islamic Republic of Iran, 4 1 (1993): e31155,
VANCOUVER
. EFFICIENT PHOSPHOROUS-SULFUR
BOND REDUCTION IN BICYCLIC
THIAPHOSPHORANES WITH
TRI-n-BUTYLTIN HYDRIDE. J. Sci. I. R. I.. 1993;4(1):e31155.