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Titolo:
2-arylsulfinylmethyl oxazines: Chiral carbonyl equivalents
Autore:
Singh, K; Deb, PK; Behal, S;
Indirizzi:
Guru Nanak Dev Univ, Dept Appl Chem Sci & Technol, Amritsar 143005, Punjab, India Guru Nanak Dev Univ Amritsar Punjab India 143005 ar 143005, Punjab, India
Titolo Testata:
HETEROCYCLES
fascicolo: 10, volume: 55, anno: 2001,
pagine: 1937 -
SICI:
0385-5414(20011001)55:10<1937:2OCCE>2.0.ZU;2-H
Fonte:
ISI
Lingua:
ENG
Soggetto:
ENANTIOSELECTIVE SYNTHESIS; ACETYLENIC SULFOXIDE;
Keywords:
Pictet-Spengler reaction; oxazinane; folate model; yohimbine alkaloid; chiral sulfoxide;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
14
Recensione:
Indirizzi per estratti:
Indirizzo: Singh, K Guru Nanak Dev Univ, Dept Appl Chem Sci & Technol, Amritsar 143005, Punjab, India Guru Nanak Dev Univ Amritsar Punjab India 143005 , Punjab, India
Citazione:
K. Singh et al., "2-arylsulfinylmethyl oxazines: Chiral carbonyl equivalents", HETEROCYCLE, 55(10), 2001, pp. 1937

Abstract

A single pot acid catalysed condensation reaction of 2-arylsulfinylmethyloxazinane - a chiral carbonyl equivalent (derived from the title oxazine by BH4- reduction) with tryptamine and tryptophan esters, furnishes tetrahydro-beta -carbolines and can be subsequently transformed into indole alkaloids.

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Documento generato il 25/01/20 alle ore 16:29:55