Literature DB >> 15816777

[Rh(CO)2Cl]2-catalyzed domino reactions involving allylic substitution and subsequent carbocyclization reactions.

Brandon L Ashfeld1, Kenneth A Miller, Anna J Smith, Kristy Tran, Stephen F Martin.   

Abstract

[reaction: see text] Three novel domino reaction processes have been discovered and developed that employ the regioselective and stereoselective [Rh(CO)(2)Cl](2)-catalyzed alkylations of allylic trifluoroacetates with alpha-substituted sodiomalonates followed by an intramolecular Pauson-Khand annulation, a [5 + 2] cycloaddition, or a cycloisomerization. A unique aspect of the methodology is that a single catalyst is used to effect sequential transformations simply by increasing the temperature for the second reaction.

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Year:  2005        PMID: 15816777     DOI: 10.1021/ol0504300

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


  4 in total

1.  Concise, enantioselective total synthesis of (-)-alstonerine.

Authors:  Kenneth A Miller; Stephen F Martin
Journal:  Org Lett       Date:  2007-02-14       Impact factor: 6.005

2.  Natural Products and Their Mimics as Targets of Opportunity for Discovery.

Authors:  Stephen F Martin
Journal:  J Org Chem       Date:  2017-09-15       Impact factor: 4.354

3.  The Pauson-Khand Reaction as a New Entry to the Synthesis of Bridged Bicyclic Heterocycles: Application to the Enantioselective Total Synthesis of (-)-Alstonerine.

Authors:  Kenneth A Miller; Charles S Shanahan; Stephen F Martin
Journal:  Tetrahedron       Date:  2008       Impact factor: 2.457

4.  Rh-catalyzed (5+2) cycloadditions of 3-acyloxy-1,4-enynes and alkynes: computational study of mechanism, reactivity, and regioselectivity.

Authors:  Xiufang Xu; Peng Liu; Xing-zhong Shu; Weiping Tang; K N Houk
Journal:  J Am Chem Soc       Date:  2013-06-14       Impact factor: 15.419

  4 in total

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