A Convenient Route to Vicinally Substituted Cyclopentanones via Pinacol Type Rearrangement of Cyclobutanes

DOI: 10.1016/0040-4039(93)88087-Y

Source and publish data:

Tetrahedron Letters p. 4565 - 4566 (1993)

Update date:2022-08-04

Topics:

Authors:

Ghosh, Subrata

Patra, Debasis

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0040-4039(93)88087-Y

A convenient route to the vicinally substituted cyclopentanones 4, 8 have been developed via rearrangement of oxabicyclo<3.2.0>heptanes obtained through intramolecular <2+2> photocycloaddition in dienes derived from ketones 1, 7.

Full text of DOI:10.1016/0040-4039(93)88087-Y

Products guided by the article

Product name:2-Ethoxy-3-(1,4-dimethylcyclohexyl)buten-3-ol

Cas No:163013-25-0

R&D Labs maybe for 163013-25-0

Xi'an Tizan Tech & Industry Co., Ltd.

Contact:86-18629066522

Address:C3009 TANG FENG INTERNATIONAL PLAZA, NO.18 FENGHUI NAN ROAD, XI'AN HIGH TECH ZONE, 710075 CHINA.
YanCheng LongShen Chemical Co.,Ltd.

Contact:+86-515-86668866

Address:No.13,Weiyi Road,Funing Aoyang Industrial Park
Acros Pharmatech Limited

website:http://www.acrospharmatech.com

Contact:+1-3234804688

Address:Flat/RM 1502,Easey Commercial building 253-261 Hennessy Road,Wanchai，HongKong
Guangzhou PI & PI Biotech Inc. Ltd.

Contact:+86-20-81716320

Address:Suite 501,198 Kaiyuan Ave.,Science City, Guangzhou,China
Shanghai Pinewood Fine Chemical Co., Ltd.

website:http://www.pinewoodchem.com

Contact:0086-21-62417129，62414096

Address:Suite B, 27F, No.2, Lane 600, Tianshan Road, Shanghai

Relevant to this article

Enantioselective Total Syntheses of the Proposed and Revised Structures of Methoxystemofoline: A Stereochemical Revision

Doi:10.1021/acs.joc.0c02667
(2021)
Synthesis and antimicrobial activity of some new substituted pyrido[3′,2′:4,5]thieno[3,2-d]-pyrimidinone derivatives

Doi:10.1134/S1068162014030042
(2014)
Carbon-heteroatom bond-forming reductive elimination. Mechanism, importance of trapping reagents, and unusual electronic effects during formation of aryl sulfides

Doi:10.1021/ja00115a033
(1995)
Doi:10.1021/jo01270a096
(1968)
Synthesis of enantiopure arylkainoids: Preparation of (2S)-Δ³-4-phenylkainic acid

Doi:10.1021/jo00114a007
(1995)
Synthesis of N-(1-nitropyren-6-yl and 8-yl)-2'-deoxyribonucleosides

Doi:10.1021/tx00047a009
(1995)

Article Doi