Literature DB >> 11405695

A rhodium carbene cyclization-cycloaddition cascade strategy toward the pseudolaric acids.

P Chiu1, B Chen, K F Cheng.   

Abstract

A rhodium carbene intramolecular cyclization-cycloaddition cascade was employed as the key reaction in the synthesis of the nucleus of the cytotoxic diterpenoids pseudolaric acids A and B.

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Year:  2001        PMID： 11405695     DOI： 10.1021/ol0159165

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


  6 in total

1.  Cycloaddition protocol for the assembly of the hexacyclic framework associated with the kopsifoline alkaloids.

Authors:  Xuechuan Hong; Stefan France; José M Mejía-Oneto; Albert Padwa
Journal:  Org Lett       Date:  2006-10-26       Impact factor: 6.005

2.  A Dipolar Cycloaddition Approach Toward the Kopsifoline Alkaloid Framework.

Authors:  Xuechuan Hong; Stefan France; Albert Padwa
Journal:  Tetrahedron       Date:  2007-06-25       Impact factor: 2.457

3.  Total synthesis of (-)-pseudolaric acid B.

Authors:  Barry M Trost; Jerome Waser; Arndt Meyer
Journal:  J Am Chem Soc       Date:  2007-11-07       Impact factor: 15.419

4.  Total synthesis of (-)-pseudolaric acid B.

Authors:  Barry M Trost; Jerome Waser; Arndt Meyer
Journal:  J Am Chem Soc       Date:  2008-12-03       Impact factor: 15.419

5.  The Rhodium(II) Carbenoid Cyclization-Cycloaddition Cascade of alpha-Diazo Dihydroindolinones for the Synthesis of Novel Azapolycyclic Ring Systems.

Authors:  Dylan B England; James M Eagan; Gokce Merey; Olcay Anac; Albert Padwa
Journal:  Tetrahedron       Date:  2008-02-04       Impact factor: 2.457

6.  Synthesis of (+/-)-3H-epivincamine via a Rh(II)-triggered cyclization/cycloaddition cascade.

Authors:  Dylan B England; Albert Padwa
Journal:  Org Lett       Date:  2007-07-21       Impact factor: 6.005
  6 in total

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