Literature DB >> 15127442

A mild method for the preparation of gamma-hydroxy-alpha,beta-acetylenic esters.

Shatrughan P Shahi1, Kazunori Koide.   

Abstract

Entities:  

Year:  2004        PMID： 15127442     DOI： 10.1002/anie.200353400

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  5 in total

1.  Total syntheses, fragmentation studies, and antitumor/antiproliferative activities of FR901464 and its low picomolar analogue.

Authors:  Brian J Albert; Ananthapadmanabhan Sivaramakrishnan; Tadaatsu Naka; Nancy L Czaicki; Kazunori Koide
Journal:  J Am Chem Soc       Date:  2007-02-06       Impact factor: 15.419

2.  Total synthesis of the Hsp90 inhibitor geldanamycin.

Authors:  Hua-Li Qin; James S Panek
Journal:  Org Lett       Date:  2008-05-20       Impact factor: 6.005

3.  The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups.

Authors:  Barry M Trost; Andrew H Weiss
Journal:  Adv Synth Catal       Date:  2009-05       Impact factor: 5.837

4.  Development of Zn-ProPhenol-catalyzed asymmetric alkyne addition: synthesis of chiral propargylic alcohols.

Authors:  Barry M Trost; Mark J Bartlett; Andrew H Weiss; Axel Jacobi von Wangelin; Vincent S Chan
Journal:  Chemistry       Date:  2012-10-23       Impact factor: 5.236

5.  Cyclic Acetal Formation Between 2-Pyridinecarboxaldehyde and gamma-Hydroxy-alpha,beta-Acetylenic Esters.

Authors:  Sami Osman; Kazunori Koide
Journal:  Tetrahedron Lett       Date:  2008-11-10       Impact factor: 2.415
  5 in total

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