Article ISI SCOPUS
SYNTHESIS-STUTTGART  (2007)

A convenient preparation of 7-bromo-2H-1,4-benzothiazine-3,5,8(4H)-trione and its application in the synthesis of the conaquinone B skeleton

Villalobos, L; Salas, C

Abstract

7-Bromo-2H-1,4-benzothiazine-3,5,8(4H)-trione was synthesized by reaction of 5-bromo-2-nitro-1,4-benzoquinone with methyl thioglycolate followed by reductive cyclization and oxidation. The Diels-Alder reaction of the product quinone with myrcene afforded the expected naphthothiazine. © Georg Thieme Verlag Stuttgart.

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Título según WOS: A convenient preparation of 7-bromo-2H-1,4-benzothiazine-3,5,8(4H)-trione and its application in the synthesis of the conaquinone B skeleton
Título según SCOPUS: A convenient preparation of 7-bromo-2H-1,4-benzothiazine-3,5,8(4H)-trione and its application in the synthesis of the conaquinone B skeleton
Título de la Revista: SYNTHESIS-STUTTGART
Número: 24
Editorial: GEORG THIEME VERLAG KG
Fecha de publicación: 2007
Página de inicio: 3773
Página final: 3775
Idioma: English
URL: http://www.thieme-connect.de/DOI/DOI?10.1055/s-2007-990895
DOI:

10.1055/s-2007-990895
Notas: ISI, SCOPUS