Literature DB >> 12943426

Formal synthesis of (-)-apicularen A.

Benjamin R Graetz1, Scott D Rychnovsky.   

Abstract

[reaction: see text] A formal synthesis of (-)-apicularen A has been completed. The synthesis features a cyanohydrin acetonide coupling as a convergent approach to the C9-C18 segment and an intramolecular Diels-Alder addition sequence to create both the 10-membered macrocycle and the aromatic ring.

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Year:  2003        PMID: 12943426     DOI: 10.1021/ol0353417

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


  2 in total

1.  De novo formal synthesis of (-)-apicularen A via an iterative asymmetric hydration sequence.

Authors:  Miaosheng Li; George A O'Doherty
Journal:  Org Lett       Date:  2006-12-21       Impact factor: 6.005

Review 2.  De novo synthesis of natural products via the asymmetric hydration of polyenes.

Authors:  Yanping Wang; Yalan Xing; Qi Zhang; George A O'Doherty
Journal:  Chem Commun (Camb)       Date:  2011-05-11       Impact factor: 6.222

  2 in total

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