Mechanistic investigations into the photochemical oxidation of thioketones

N. Ramnath, V. Ramesh, Vaidhyanathan Ramamurthy

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Singlet-oxygen reaction with dialkyl, aryl alkyl, and diaryl thioketones is found to give the corresponding sulphines and ketones in proportions depending on the nature of the thioketone.

Original languageEnglish
Pages (from-to)112-114
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number3
StatePublished - Dec 1 1981
Externally publishedYes

Fingerprint

Singlet Oxygen
Ketones
Oxidation

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Mechanistic investigations into the photochemical oxidation of thioketones. / Ramnath, N.; Ramesh, V.; Ramamurthy, Vaidhyanathan.

In: Journal of the Chemical Society, Chemical Communications, No. 3, 01.12.1981, p. 112-114.

Research output: Contribution to journalArticle

@article{0631af7a5b3f4079b28af496c89e3b97,
title = "Mechanistic investigations into the photochemical oxidation of thioketones",
abstract = "Singlet-oxygen reaction with dialkyl, aryl alkyl, and diaryl thioketones is found to give the corresponding sulphines and ketones in proportions depending on the nature of the thioketone.",
author = "N. Ramnath and V. Ramesh and Vaidhyanathan Ramamurthy",
year = "1981",
month = "12",
day = "1",
language = "English",
pages = "112--114",
journal = "Journal of the Chemical Society",
issn = "0577-6171",
publisher = "Chemical Society",
number = "3",

}

TY - JOUR

T1 - Mechanistic investigations into the photochemical oxidation of thioketones

AU - Ramnath, N.

AU - Ramesh, V.

AU - Ramamurthy, Vaidhyanathan

PY - 1981/12/1

Y1 - 1981/12/1

N2 - Singlet-oxygen reaction with dialkyl, aryl alkyl, and diaryl thioketones is found to give the corresponding sulphines and ketones in proportions depending on the nature of the thioketone.

AB - Singlet-oxygen reaction with dialkyl, aryl alkyl, and diaryl thioketones is found to give the corresponding sulphines and ketones in proportions depending on the nature of the thioketone.

UR - http://www.scopus.com/inward/record.url?scp=33846553531&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33846553531&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:33846553531

SP - 112

EP - 114

JO - Journal of the Chemical Society

JF - Journal of the Chemical Society

SN - 0577-6171

IS - 3

ER -