Literature DB >> 19445488

Tandem alkylation-Michael addition to vinylogous carbonates for the stereoselective construction of 2,3,3,6-tetrasubstituted tetrahydropyrans.

Santosh J Gharpure1, S Raja Bhushan Reddy.   

Abstract

A stereoselective method for the synthesis of substituted tetrahydropyran derivatives employing a tandem S(N)2-Michael addition sequence to vinylogous carbonates is developed. The method is extended to the synthesis of bicyclic ether motifs present in polyether ladder toxins.

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Year:  2009        PMID: 19445488     DOI: 10.1021/ol900721q

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


  2 in total

1.  Asymmetric Total Synthesis of the Indole Diterpene Alkaloid Paspaline.

Authors:  Robert J Sharpe; Jeffrey S Johnson
Journal:  J Org Chem       Date:  2015-10-02       Impact factor: 4.354

2.  Trianion synthon approach to spirocyclic heterocycles.

Authors:  Matthew A Perry; Richard R Hill; Scott D Rychnovsky
Journal:  Org Lett       Date:  2013-04-17       Impact factor: 6.005

  2 in total

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