Literature DB >> 28906071

Construction of Quaternary Stereogenic Centers in the Total Synthesis of Natural Products.

Evgeny V Prusov1.   

Abstract

Total syntheses of the tetracyclic terpene waihoensene and the densely functionalized tetracyclic compound ryanodol have recently been reported. Both approaches constitute examples of the efficient and innovative construction of multiple quaternary centers.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  natural products; quaternary stereocenters; radical cyclization; terpenoids; total synthesis

Year:  2017        PMID: 28906071     DOI: 10.1002/anie.201706629

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Stereoselective α-Tertiary Alkylation of N-(Arylacetyl)oxazolidinones.

Authors:  Eunjae Shim; Armen Zakarian
Journal:  Synlett       Date:  2020-04       Impact factor: 2.454

2.  Desymmetrization of meso-bisphosphates using copper catalysis and alkylzirconocene nucleophiles.

Authors:  Reece Jacques; Robert D C Pullin; Stephen P Fletcher
Journal:  Nat Commun       Date:  2019-01-03       Impact factor: 14.919

  2 in total

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