Literature DB >> 15116221

Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts.

Nakcheol Jeong1, Dong Hoon Kim, Jun Hun Choi.   

Abstract

Desymmetrization of the meso dienynes, such as propargyl 1-vinylallyl N-tosylamides (1a-c) and propargyl 1-vinylallyl ethers (1d-e), by asymmetric Pauson-Khand type reaction catalysts was studied. The corresponding vinyl substituted bicyclic pentenones (2 and 3) were obtained with high diastereoselectivity and enantioselectivity.

Entities:  

Year:  2004        PMID: 15116221     DOI: 10.1039/b401288g

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


  3 in total

1.  Enantioselective synthesis of 5,7-bicyclic ring systems from axially chiral allenes using a Rh(I)-catalyzed cyclocarbonylation reaction.

Authors:  Francois Grillet; Kay M Brummond
Journal:  J Org Chem       Date:  2013-03-29       Impact factor: 4.354

Review 2.  Application of Pauson-Khand reaction in the total synthesis of terpenes.

Authors:  Majid M Heravi; Leila Mohammadi
Journal:  RSC Adv       Date:  2021-11-29       Impact factor: 4.036

3.  Iridium-catalyzed intramolecular [4 + 2] cycloadditions of alkynyl halides.

Authors:  Andrew Tigchelaar; William Tam
Journal:  Beilstein J Org Chem       Date:  2012-10-16       Impact factor: 2.883

  3 in total

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