Literature DB >> 15932211

Progress toward the total synthesis of saudin: development of a tandem Stille-oxa-electrocyclization reaction.

Uttam K Tambar1, Taichi Kano, Brian M Stoltz.   

Abstract

[reaction: see text] A diastereoselective tandem Stille-oxa-electrocyclization reaction provides access to the core of the diterpenoid natural product saudin. Additionally, this new reaction sequence was extended to the convergent preparation of related polycyclic pyran systems.

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Year:  2005        PMID： 15932211     DOI： 10.1021/ol050705b

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


  5 in total

1.  Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin.

Authors:  Michael R Krout; Christopher E Henry; Thomas Jensen; Kun-Liang Wu; Scott C Virgil; Brian M Stoltz
Journal:  J Org Chem       Date:  2018-01-23       Impact factor: 4.354

2.  Studies Culminating in the Total Synthesis and Determination of the Absolute Configuration of (-)-Saudin.

Authors:  Robert K Boeckman; Maria Rico Del Rosario Ferreira; Lorna H Mitchell; Pengcheng Shao; Michael J Neeb; Yue Fang
Journal:  Tetrahedron       Date:  2011-09-21       Impact factor: 2.457

3.  Broad Spectrum Enolate Equivalent for Catalytic Chemo-, Diastereo-, and Enantioselective Addition to N-Boc Imines.

Authors:  Barry M Trost; Chao-I Joey Hung
Journal:  J Am Chem Soc       Date:  2015-12-14       Impact factor: 15.419

4.  No acid required: 4π and 6π electrocyclization reactions of dienyl diketones for the synthesis of cyclopentenones and 2H-Pyrans.

Authors:  Steven D Jacob; Joshua L Brooks; Alison J Frontier
Journal:  J Org Chem       Date:  2014-10-17       Impact factor: 4.354

Review 5.  Recent Advances in the Synthesis of 2H-Pyrans.

Authors:  David Tejedor; Fernando García-Tellado; Samuel Delgado-Hernández; Raquel Diana-Rivero; Abián Díaz-Díaz
Journal:  Molecules       Date:  2019-08-09       Impact factor: 4.411
  5 in total

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