Literature DB >> 20174450

An Ionic Diels-Alder Route to cis-Fused Octalins Containing an All-Carbon Quaternary Stereocenter in an Angular Position.

Jun Hee Lee1, Woo Han Kim, Samuel J Danishefsky.   

Abstract

We describe herein the development of efficient and stereoselective synthetic routes to a series of cis-octalins possessing an all-carbon quaternary center in an angular position.

Entities:  

Year:  2010        PMID： 20174450      PMCID： PMC2822275          DOI： 10.1016/j.tetlet.2009.12.127

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN： 0040-4039            Impact factor:   2.415


  5 in total

1.  Stereoselective synthesis of secondary organozinc reagents and their reaction with heteroatomic electrophiles.

Authors:  E Hupe; P Knochel
Journal:  Org Lett       Date:  2001-01-11       Impact factor: 6.005

2.  Syntheses of Isomerically Pure Reference Octalins and Hydrindanes.

Authors:  Jun Hee Lee; Woo Han Kim; Samuel J Danishefsky
Journal:  Tetrahedron Lett       Date:  2009-09-30       Impact factor: 2.415

3.  Formal enantioselective Michael addition with umpolung of reactivity.

Authors:  E Hupe; P Knochel
Journal:  Angew Chem Int Ed Engl       Date:  2001       Impact factor: 15.336

4.  Catalytic asymmetric synthesis of all-carbon quaternary stereocenters.

Authors:  Christopher J Douglas; Larry E Overman
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-14       Impact factor: 11.205

5.  Improved dienophilicity of nitrocycloalkenes: prospects for the development of a trans-Diels-Alder paradigm.

Authors:  Woo Han Kim; Jun Hee Lee; Samuel J Danishefsky
Journal:  J Am Chem Soc       Date:  2009-09-09       Impact factor: 15.419
  5 in total
  1 in total

1.  A Diels-Alder Route to Angularly Functionalized Bicyclic Structures.

Authors:  Woo Han Kim; Jun Hee Lee; Baptiste Aussedat; Samuel J Danishefsky
Journal:  Tetrahedron       Date:  2010-08-01       Impact factor: 2.457
  1 in total

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