Intramolecular 1,4-Addition of α-Heteroatom-Substituted Radicals to β,β-Disubstituted Enones. Applications to Tandem Cyclizations

DOI: 10.1021/ja00026a030

Source and publish data:

Journal of the American Chemical Society p. 9864 - 9865 (1991)

Update date:2022-09-26

Topics:

Authors:

Kim, Seongkon

Fuchs, P. L.

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

Article abstract of DOI:10.1021/ja00026a030

Full text of DOI:10.1021/ja00026a030

Products guided by the article

Product name:C₂₆H₃₄O₄Se

Cas No:137720-59-3

R&D Labs maybe for 137720-59-3

Hangzhou Pharma & Chem Co.,Ltd.

Contact:+86-571-87040515

Address:No,139Qingchun Rd
LINYI FUDE FINE CHEMICAL CO.,LTD

Contact:86-539-2361184

Address:YISHUI, LINYI,SAHNDONG,CHINA
AstaTech ( Chengdu) BioPharmaceutical Corp.

website:http://www.astabiochem.cn/

Contact:+86-15198215156-15198215156

Address:SICHUAN CHENGDU
Shanggao Ruiya Fine Chemicals Co., Ltd

Contact:+86-795-2592103

Address:Xingguang Nanlu,Shanggao County Industry Park
Guangzhou Reachin Chemical Co., Ltd

Contact:+86-20-37087379 ext.604

Address:A122C-1, Tianyuan Plaza, 401 Tianyuan Rd., Tianhe, Guangzhou, China

Relevant to this article

Does diatomic sulfur (S₂) react as a free species?

Doi:10.1021/ja00030a048
(1992)
Transition-metal-promoted conversion of dichlorovinylcyclobutanes to cyclohexadienes

Doi:10.1021/om00037a071
(1992)
Synthesis and anticancer activity of 5,6,8,13-tetrahydro-7Hnaphtho[2,3-a] [3]-benzazepine-8,13-diones

Doi:10.1007/s12272-012-0502-3
(2012)
Polymer-supported stereoselective synthesis of benzimidazolinopiperazinones

Doi:10.1021/jo300836c
(2012)
Synthesis and anxiolytic activity of N-substituted cyclic imides (1R*,2S*3R*,4S*)-N-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-2,3-b icyclo[2.2.1]heptanedicarboxime (Tandospirone) and related compounds

Doi:10.1248/cpb.39.2288
(1991)
Synthesis, characterization, and biological evaluation of certain 1,3-thiazolone derivatives bearing pyrazoline moiety as potential anti-breast cancer agents

Doi:10.1007/s00044-012-0098-7
(2013)

Article Doi