Literature DB >> 17658853

Highly enantioselective synthesis of beta-amino alcohols: a catalytic version.

Thomas-Xavier Métro1, Domingo Gomez Pardo, Janine Cossy.   

Abstract

Highly enantioselective rearrangement of beta-amino alcohols was realized by using a catalytic amount of trifluoroacetic anhydride.

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Year:  2007        PMID： 17658853     DOI： 10.1021/jo071028x

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  4 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

2.  Development of Stereocontrolled Palladium(II)-Catalyzed Domino Heck/Suzuki β,α-Diarylation Reactions with Chelating Vinyl Ethers and Arylboronic Acids.

Authors:  Alejandro Trejos; Luke R Odell; Mats Larhed
Journal:  ChemistryOpen       Date:  2012-02       Impact factor: 2.911

Review 3.  Facile and Green Synthesis of Saturated Cyclic Amines.

Authors:  Arruje Hameed; Sadia Javed; Razia Noreen; Tayyaba Huma; Sarosh Iqbal; Huma Umbreen; Tahsin Gulzar; Tahir Farooq
Journal:  Molecules       Date:  2017-10-12       Impact factor: 4.411

Review 4.  Synthetic Applications of Aziridinium Ions.

Authors:  Jala Ranjith; Hyun-Joon Ha
Journal:  Molecules       Date:  2021-03-22       Impact factor: 4.411
  4 in total

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