Iodomethyl phenyl sulfoxide: reactivity and synthetic applications

Lithio iodomethyl phenyl sulfoxides reacted with alkyl halides and carbonyl compounds to give adducts in good to moderate yields. Solvolysis of the carbonyl adducts led to sulfones or the ring expanded product. © 1984.

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Main Authors: Vichai Reutrakul, Chitchanun Panyachotipun, Viwat Hahnvajanawong, S. Sotheeswaran
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/30586
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spelling th-mahidol.305862018-10-12T14:44:49Z Iodomethyl phenyl sulfoxide: reactivity and synthetic applications Vichai Reutrakul Chitchanun Panyachotipun Viwat Hahnvajanawong S. Sotheeswaran Mahidol University University of Peradeniya Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Lithio iodomethyl phenyl sulfoxides reacted with alkyl halides and carbonyl compounds to give adducts in good to moderate yields. Solvolysis of the carbonyl adducts led to sulfones or the ring expanded product. © 1984. 2018-10-12T07:40:24Z 2018-10-12T07:40:24Z 1984-01-01 Article Tetrahedron Letters. Vol.25, No.17 (1984), 1825-1828 10.1016/S0040-4039(01)90051-6 00404039 2-s2.0-48749133877 https://repository.li.mahidol.ac.th/handle/123456789/30586 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=48749133877&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Vichai Reutrakul
Chitchanun Panyachotipun
Viwat Hahnvajanawong
S. Sotheeswaran
Iodomethyl phenyl sulfoxide: reactivity and synthetic applications
description Lithio iodomethyl phenyl sulfoxides reacted with alkyl halides and carbonyl compounds to give adducts in good to moderate yields. Solvolysis of the carbonyl adducts led to sulfones or the ring expanded product. © 1984.
author2 Mahidol University
author_facet Mahidol University
Vichai Reutrakul
Chitchanun Panyachotipun
Viwat Hahnvajanawong
S. Sotheeswaran
format Article
author Vichai Reutrakul
Chitchanun Panyachotipun
Viwat Hahnvajanawong
S. Sotheeswaran
author_sort Vichai Reutrakul
title Iodomethyl phenyl sulfoxide: reactivity and synthetic applications
title_short Iodomethyl phenyl sulfoxide: reactivity and synthetic applications
title_full Iodomethyl phenyl sulfoxide: reactivity and synthetic applications
title_fullStr Iodomethyl phenyl sulfoxide: reactivity and synthetic applications
title_full_unstemmed Iodomethyl phenyl sulfoxide: reactivity and synthetic applications
title_sort iodomethyl phenyl sulfoxide: reactivity and synthetic applications
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/30586
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