Photo-induced transformations. Part 51. Photo- and thermally-induced rearrangements of hypoiodites of steroidal homoallyl alcohols. The formation of some oxygen heterocycles via photo- and thermally-induced rearrangements of 3-hydroxy-Δ5-steroid hypoiodites in the presence of mercury(II) oxide and iodine-Reference-Cited by-同舟云学术

Photo-induced transformations. Part 51. Photo- and thermally-induced rearrangements of hypoiodites of steroidal homoallyl alcohols. The formation of some oxygen heterocycles via photo- and thermally-induced rearrangements of 3-hydroxy-Δ5-steroid hypoiodites in the presence of mercury(II) oxide and iodine

Published:1981 Issue:0 Volume: Page:236-250
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,Furusaki Akio,Kato Kimitoshi,Maeda Norio,Yonebayashi Fumihiko

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1981/P1/P19810000236

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. β-Scission of Alkoxy Radicals in Synthetic Transformations;Chemistry Letters;2017-12-05

2. First total synthesis of (±)-3-aza-11-oxa-1,3,5(10)-trieno steroids;Steroids;2006-10

3. Radical-mediated ring enlargement of cyclobutenones: new synthetic potential of squaric acid.;Journal of the American Chemical Society;1995-09

4. Photoinduced molecular transformations. Part 155. General synthesis of macrocyclic ketones based on a ring expansion involving a selective β-scission of alkoxyl radicals, its application to a new synthesis of (±)-isocaryophyllene and (±)-caryophyllene, and a conformational analysis of the two sesquiterpenes and the radical intermediate in the synthesis by MM3 calculations;J. Chem. Soc., Perkin Trans. 1;1995

5. 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;J. Chem. Soc., Perkin Trans. 1;1995