Literature DB >> 17760451

A [3 + 3] annelation approach to (+)-rhopaloic acid B.

Julien C R Brioche1, Katharine M Goodenough, David J Whatrup, Joseph P A Harrity.   

Abstract

A general and enantiospecific [3 + 3] reaction toward functionalized pyrans is reported that has been employed in the first enantioselective synthesis of (+)-rhopaloic acid B.

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Year:  2007        PMID： 17760451     DOI： 10.1021/ol701553j

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


  5 in total

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Authors:  Chenlong Zhang; Weipeng Hu; James P Morken
Journal:  ACS Catal       Date:  2021-08-12       Impact factor: 13.700

3.  Constructing the Architecturally Distinctive ABD-Tricycle of Phomactin A through an Intramolecular Oxa-[3 + 3] Annulation Strategy.

Authors:  Grant S Buchanan; Kevin P Cole; Gang Li; Yu Tang; Ling-Feng You; Richard P Hsung
Journal:  Tetrahedron       Date:  2011-12-30       Impact factor: 2.457

4.  Catalytic SN2'- and Enantioselective Allylic Substitution with a Diborylmethane Reagent and Application in Synthesis.

Authors:  Ying Shi; Amir H Hoveyda
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-04       Impact factor: 15.336

5.  Iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones to chiral diols.

Authors:  Xiao-Hui Yang; Hai-Tao Yue; Na Yu; Yi-Pan Li; Jian-Hua Xie; Qi-Lin Zhou
Journal:  Chem Sci       Date:  2016-11-15       Impact factor: 9.825
  5 in total

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