Preparation of alkyl-substituted indoles in the benzene portion. Part 10. Synthesis of 4- and/or 5-alkylated 1,6,7,8-tetrahydrocyclopent[g]indoles, model compounds for herbindole and trikentrin syntheses

DOI: 10.1248/cpb.42.846

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 846 - 853 (1994)

Update date:2022-08-03

Topics: Synthesis Syntheses Model compounds

Authors:

Muratake

Mikawa Mikawa

Seino Seino

Natsume Natsume

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

Article abstract of DOI:10.1248/cpb.42.846

Synthetic pathways leading to model compounds 25, 27, 33, 20d, 32b, 37, and 42 for the marine alkaloids, herbindoles and trikentrins (1b-i), are presented. p-Toluenesulfonic acid-mediated indole cyclization reactions, 19→20 and 38→39, assisted with thiols

Full text of DOI:10.1248/cpb.42.846

NII-Electronic Library Service

Products guided by the article

Product name:methyl 1-(phenylsulfonyl)-1,6,7,8-tetrahydrocyclopentindole-5-carboxylate

Cas No:157331-69-6

R&D Labs maybe for 157331-69-6

Beijing Chemdow Co., Ltd

website:http://www.chemdow.com

Contact:0086-10-82435335

Address:Room 401,Unit 3,4th Floor,Shangdijiayuan,Shangdi East Road, Haidian District,Beijing
Tianjin Chemsyntech Chemical Co., Ltd

Contact:+86-22-60872258

Address:Haitai green industry base in Tianjin, K1,5-601
HANWAYS CHEMPHARM CO.,LIMITED

website:http://www.hanwayschem.com

Contact:+86-18502787239(whatsapp)

Address:18-1-802, Green Garden, Jianghan District, Wuhan 430023, China
Hunan Haili Chemical Industry Co.,Ltd.

Contact:+86-731-85521860

Address:No.251, 2nd Section, Furong Road, Changsha,Hunan,China
Nanjing Duly Biotech Co., Ltd

website:http://www.dulynet.com/

Contact:025-84699383 -8003

Address:Room 503, Building 2, Chuangxinhui, No. 61 Wenjing Road, High-tech Development Zone, Pukou District, Nanjing City, Jiangsu Province Nanjing, Jiangsu

Relevant to this article

Stereoselective control in the Staudinger reactions involving monosubstituted ketenes with electron acceptor substituents: Experimental investigation and theoretical rationalization

Doi:10.1039/c0ob00783h
(2011)
Synthesis of New Homochiral Polyfunctionalized Furan-2(5H)-ones

Doi:10.1016/0957-4166(94)80182-7
(1994)
NHC-coordinated silagermenylidene functionalized in allylic position and its behaviour as a ligand

Doi:10.1039/c4dt00094c
(2014)
Synthesis of the core structure of apicularen a by transannular cyclization.

Doi:10.1021/ol017261d
(2002)
The preparation and phosphorylation of 2,5- and 1D-2,6-di-O-benzyl-myo-inositol

Doi:10.1016/S0008-6215(00)90549-4
(1992)
A catalytic asymmetric synthesis of hydrindans

Doi:10.1016/S0040-4039(00)92252-4
(1992)

Article Doi