One-step formation of furo[3,2-c]quinolin-4(5H)-ones by a new regioselective [2+3] photoaddition of methoxy-substituted 4-hydroxyquinolin-2-one with alkenes1-Reference-Cited by-同舟云学术

One-step formation of furo[3,2-c]quinolin-4(5H)-ones by a new regioselective [2+3] photoaddition of methoxy-substituted 4-hydroxyquinolin-2-one with alkenes1

Published:1991-09 Issue:38 Volume:32 Page:5115-5118
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Suginome Hiroshi,Seko Shinzo,Konishi Atsushi,Kobayashi Kazuhiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. The photoaddition of 4-hydroxycoumarin andN-methyl-4-hydroxyquinol-2-one to cyclohexene.

2. A photochemical synthesis of 1,2,3,4,5,6-hexahydro-1-benzazocine-2,6-diones from 4-hydroxy-2-quinolones.

3. Photoinduced molecular transformations. 110. Formation of furoquinolinones via .beta.-scission of cyclobutanoxyl radicals generated from [2 + 2] photoadducts of 4-hydroxy-2-quinolone and acyclic and cyclic alkenes. X-ray crystal structure of (6a.alpha.,6b.beta.,10a.beta.,10b.alpha.)-(.+-.)-10b-acetoxy-6a,6b,7,8,9,10,10a,10b-octahydro-5-methylbenzo[3,4]cyclobuta[1,2-c]quinolin-6(5H)-one

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