Literature DB >> 12357800

Structure and chemistry of a zwitterionic amine-aldehyde adduct.

Anthony J Kirby1, Igor V Komarov, Vitaliy A Bilenko, John E Davies, Jeremy M Rawson.   

Abstract

The zwitterionic tetrahedral addition product 1 is the preferred form of the amino-aldehyde 4 in polar solvents and in the crystal, where a molecule of water controls the structure.

Entities:  

Year:  2002        PMID： 12357800     DOI： 10.1039/b206639d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

Review 1.  Chemistry of bridged lactams and related heterocycles.

Authors:  Michal Szostak; Jeffrey Aubé
Journal:  Chem Rev       Date:  2013-06-17       Impact factor: 60.622

2.  Proximity effects in nucleophilic addition reactions to medium-bridged twisted lactams: remarkably stable tetrahedral intermediates.

Authors:  Michal Szostak; Lei Yao; Jeffrey Aubé
Journal:  J Am Chem Soc       Date:  2010-02-17       Impact factor: 15.419

3.  Construction of an advanced tetracyclic intermediate for total synthesis of the marine alkaloid sarain A.

Authors:  Sungwoo Hong; Jinhai Yang; Steven M Weinreb
Journal:  J Org Chem       Date:  2006-03-03       Impact factor: 4.354
  3 in total

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