Photoinduced molecular transformations. Part 152. Ring expansion based on a sensitized [2 + 2] photoaddition of enol ethers of cyclic ketones with olefins, followed by a β-scission of alkoxyl radicals generated from the resulting cyclobutanols. Two-carbon ring expansion of β-indanone, β-tetralone and β-suberone-Reference-Cited by-同舟云学术

Photoinduced molecular transformations. Part 152. Ring expansion based on a sensitized [2 + 2] photoaddition of enol ethers of cyclic ketones with olefins, followed by a β-scission of alkoxyl radicals generated from the resulting cyclobutanols. Two-carbon ring expansion of β-indanone, β-tetralone and β-suberone

Published:1995 Issue:1 Volume: Page:49-61
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Suginome Hiroshi,Takeda Toshihiro,Itoh Masahito,Nakayama Yutaka,Kobayashi Kazuhiro

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1995/P1/P19950000049

Reference50 articles.

1. Photoinduced molecular transformations. Part 151. One-pot synthesis of 1H-benz[g]indole-4,5-diones by a regioselective (3+2) photoaddition of 4

2. Ring Expansion through [2+2] Photocycloaddition–β-Scission Sequence. Two Carbon Ring Expansions of β-Indanone and β-Tetralone

3. Photoinduced transformations. Part 73. Transformations of five- (and six-) membered cyclic alcohols into five- (and six-) membered cyclic ethers - a new method of a two-step transformation of hydroxy steroids into oxasteroids

4. Photoinduced transformations. 76. A four-step substitution of a carbonyl group of steroidal ketones by an oxygen atom. A new method for the synthesis of cyclic ethers

5. Photoinduced molecular transformations. Part 107. A versatile substitution of a carbonyl group of steroidal ketones by a heteroatom. The synthesis of aza-, oxa-, thia-, selena-, and tellurasteroids

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