Effect of N-Chloro Structure and 1-Substituent on ?-Substitution (Addition - Elimination) in Pyrroles

DOI: 10.1021/jo00283a032

Source and publish data:

Journal of Organic Chemistry p. 5347 - 5350 (1989)

Update date:2022-08-06

Topics:

Authors:

Rosa, Michael De

Nieto, Gustavo Cabrera

Gago, Fernando Ferrer

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

Article abstract of DOI:10.1021/jo00283a032

1-Methylpyrrole was reacted with a number of different types of N-chloro derivatives, and ?-substitution was observed only with N-chloroimides.It is proposed that there is qualitative relationship between the pK_a of the N-chloro precursor and t

Full text of DOI:10.1021/jo00283a032

Products guided by the article

Product name:N-(1-benzyl-1H-pyrrol-2-yl)succinimide

Cas No:122845-04-9

R&D Labs maybe for 122845-04-9

Shijiazhuang Yunxuan Im&Export Co.,Ltd.

Contact:+86-311-83037514

Address:No.6 Hongbin Road
Hongyi Import & Export CO.,LTD

Contact:86-13319649499

Address:Nanzheng Neighborhood Commitees, Chongwen Office, Yongding District
Wuxi Highness Chemical Co.,Ltd

website:https://www.phtpharmatech.com/

Contact:86-510-81771080

Address:No58 East Xinguan Rd, Guanlin Town, Yixing City, Jiangsu China
Ningbo J&S Botanics Inc.

Contact:86-574-26865651

Address:529 YuanBaoShan Road, Beilun District
Ningbo Inno Pharmchem Co., Ltd.

Contact:86-574-87319282

Address:6F-5,NO.163 RUIQING RD.,NINGBO 315000 CHINA

Relevant to this article

Asymmetrie synthesis of α,β-Diaminophosphonic acid derivatives with a catalytic enantioselective mannich reaction

Doi:10.1002/adsc.200900208
(2009)
Synthesis, anticoagulant and PIVKA-II induced by new 4-hydroxycoumarin derivatives

Doi:10.1016/j.bmc.2010.04.009
(2010)
Organocatalytic kinetic resolution via intramolecular aldol reactions: Enantioselective synthesis of both enantiomers of chiral cyclohexenones

Doi:10.1039/b927343c
(2010)
Tetrahedral and square planar Ni[(SPR₂)₂N] ₂ complexes, R = Ph &ⁱPr revisited: Experimental and theoretical analysis of interconversion pathways, structural preferences, and spin delocalization

Doi:10.1021/ic100163g
(2010)
N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID AS A NEW REAGENT FOR THE SELECTICE CLEVEAGE OF ACTIVE ESTERS UNDER NEUTRAL CONDITIONS

Doi:10.1016/S0040-4039(00)95161-X
(1989)
Preparation of cyanoguanidine and ethylcyanamide complexes of ruthenium(II) and osmium(II)

Doi:10.1002/ejic.200900639
(2009)

Article Doi