Tetrapyrroles. IV. A highly efficient synthesis of homochiral dihydropyrromethenones via Pd○ mediated coupling of iodopyrroles and acetylenic amides

DOI: 10.1016/S0040-4039(00)60941-3

Source and publish data:

Tetrahedron Letters p. 6235 - 6238 (1992)

Update date:2022-08-04

Topics:

Authors:

Jacobi, Peter A.

Rajeswari

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

Article abstract of DOI:10.1016/S0040-4039(00)60941-3

Homochiral dihydropyrromethenones of type 20 have been synthesized in a highly efficient manner by Pd^○ mediated coupling of iodopyrrole 14 with acetylenic amides 18, followed by F- catalyzed 5-exo-dig cyclization. In analogous fashion, phytochr

Full text of DOI:10.1016/S0040-4039(00)60941-3

Products guided by the article

Product name:2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-[[5-oxo-1-(phenylmethyl)-2-pyrrolidinylidene]methyl] -, methyl ester, (Z)-

Cas No:145100-14-7

R&D Labs maybe for 145100-14-7

Hefei EnliPharma Tecnology Co.,Ltd

Contact:0086-551-66399836

Address:Qing Cheng ShuiXiang Building 805, Mengcheng North Road , ShuangFeng Economic Development Zone Anhui HeFei
Tianjin Jingye Fine Chemicals Co., Ltd.

Contact:+86-15722078107; +86-22-26911407

Address:Bohua Fine Chemicals Base of Petrochemical Industry Park, Nanhuan Road, Dagang District, Tianjin, 300271, P. R. China
Hotechem Shanghai Co., Ltd

Contact:13120882795；+86-21-34621078;+86-021-31122318

Address:Suite 2,No.2715 Longwu Road
Shanghai Xinda Pharmaceuticals Co., Ltd.

Contact:86-21-33692333-8008

Address:999 Linxian Road, Jinshan Industrial Park, Shanghai, China
HOST COUNTRY LIMITED

Contact:+852 83038667

Address:Room 1502, 15th Floor, SPA Centre,53-55 Lockhart Road, Wanchai, Hong Kong

Relevant to this article

Synthesis and biological properties of novel pyridinioalkanoyl thiolesters (PATE) as anti-HIV-1 agents that target the viral nucleocapsid protein zinc fingers

Doi:10.1021/jm9802517
(1999)
Rapid synthesis of etherimides via catalytic arylation of silylated phenols

Doi:10.1016/S0040-4039(98)02505-2
(1999)
Structure-immunosuppressive activity relationships of new analogues of 15-deoxyspergualin. 1. Structural modifications of the hydroxyglycine moiety

Doi:10.1021/jm980431g
(1999)
Doi:10.1021/jo00826a050
(1970)
Visible-Light-Promoted Generation of α-Ketoradicals from Vinyl-bromides and Molecular Oxygen: Synthesis of Indenones and Dihydroindeno[1,2-c]chromenes

Doi:10.1002/anie.201702953
(2017)
Doi:10.1016/S0040-4020(01)99455-4
(1969)

Article Doi