Photochemistry of aromatic thiol esters

JR Grunwell, NA Marron, SI Hanhan

Index: Grunwell,J.R. et al. Journal of Organic Chemistry, 1973 , vol. 38, # 8 p. 1559 - 1562

Full Text: HTML

Citation Number: 20

Abstract

We found that the photolysis of 4-tolyl thiolacetate gave 4-tolyl disulfide and methyl 4-tolyl sulfide but no 4-toluenethiol nor any photo-Fries rearrangement.2 Subsequently, Bradshaw and coworkers3 reported the major products of the photolysis of phenyl thiolacetate to be phenyl disulfide, methyl phenyl sulfide, and thio- phenol, which arises from secondary photolysis of phenyl disulfide without the intervention of sol~ent,~ plus minor amounts of the corresponding photo-Fries prod- ...

Related Articles:

Reductive dimerization of organic thiocyanates to disulfides mediated by tetrathiomolybdate

[Prabhu, Kandikere R.; Ramesha, A. R.; Chandrasekaran, Srinivasan Journal of Organic Chemistry, 1995 , vol. 60, # 22 p. 7142 - 7143]

Regiocontrolled synthesis of enantiopure 3, 3'-thiosubstituted biphenyls

[Capozzi, Giuseppe; Falciani, Chiara; Menichetti, Stefano; Nativi, Cristina Gazzetta Chimica Italiana, 1996 , vol. 126, # 4 p. 227 - 232]

2-(tert. amino)-11-(4-methylpiperazino) dibenzo [b, f] thiepins and their 10, 11-dihydro derivatives; Synthesis and neuroleptic activity

[Kmonicek, Vojtech; Holubek, Jiri; Svatek, Emil; Metysova, Jirina; Protiva, Miroslav Collection of Czechoslovak Chemical Communications, 1987 , vol. 52, # 3 p. 793 - 803]

More Articles...