Literature DB >> 17764194

Catalytic activation of the leaving group in the S(N)2 reaction.

Hirofumi Yamamoto1, Ghanshyam Pandey, Yumiko Asai, Mayo Nakano, Atsushi Kinoshita, Kosuke Namba, Hiroshi Imagawa, Mugio Nishizawa.   

Abstract

A novel catalytic activation of the leaving group in the S(N)2 reaction is achieved as an extension of our mercuric triflate-catalyzed reactions. Derivatives of anilinoethyl 4-pentynoate reacted smoothly with catalytic amounts of Hg(OTf)(2) to give indoline derivatives in excellent yield with efficient catalytic turnovers under very mild conditions. The reaction of optically pure secondary alcohol derivatives resulted in inversion of stereochemistry, which is a definitive feature of the S(N)2 reaction. The procedure is applicable for benzoazepine synthesis.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17764194     DOI: 10.1021/ol701737x

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Toward palau'amine: Hg(OTf)2-catalyzed synthesis of the cyclopentane core.

Authors:  Kosuke Namba; Yukari Kaihara; Hirofumi Yamamoto; Hiroshi Imagawa; Keiji Tanino; Robert M Williams; Mugio Nishizawa
Journal:  Chemistry       Date:  2009-07-06       Impact factor: 5.236

2.  Synthesis of indolines via a domino Cu-catalyzed amidation/cyclization reaction.

Authors:  Ana Minatti; Stephen L Buchwald
Journal:  Org Lett       Date:  2008-06-04       Impact factor: 6.005

3.  Stereoinversion of Unactivated Alcohols by Tethered Sulfonamides.

Authors:  Paul T Marcyk; Latisha R Jefferies; Deyaa I AbuSalim; Maren Pink; Mu-Hyun Baik; Silas P Cook
Journal:  Angew Chem Int Ed Engl       Date:  2019-01-15       Impact factor: 15.336

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.