Literature DB >> 19527042

Synthesis of the tetracyclic core of the neomangicols using a late-stage indene alkylation.

Jessica L Wood1, Brian G Pujanauski, Richmond Sarpong.   

Abstract

A general approach to the tetracyclic core of the neomangicol natural products via a late-stage indene alkylation reaction is presented. This strategy sets the stage for access to the neomangicol family and, in addition, provides a potential biogenetically inspired entry to the mangicol natural products.

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Year:  2009        PMID： 19527042      PMCID： PMC2720047          DOI： 10.1021/ol9010008

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


  4 in total

1.  Enantioselective synthesis of the spirotetracyclic carbon core of mangicols by using a stereoselective transannular Diels-Alder strategy.

Authors:  Keisuke Araki; Keiji Saito; Hirokazu Arimoto; Daisuke Uemura
Journal:  Angew Chem Int Ed Engl       Date:  2004-01       Impact factor: 15.336

2.  Synthesis of novel spinosyn A analogues by Pd-mediated transformations.

Authors:  Lutz F Tietze; Gordon Brasche; Alexander Grube; Niels Böhnke; Christian Stadler
Journal:  Chemistry       Date:  2007       Impact factor: 5.236

3.  Mangicols: structures and biosynthesis of A new class of sesterterpene polyols from a marine fungus of the genus Fusarium.

Authors:  M K Renner; P R Jensen; W Fenical
Journal:  J Org Chem       Date:  2000-08-11       Impact factor: 4.354

4.  Benzo[b]fluorenes via indanone dianion annulation: a short synthesis of prekinamycin.

Authors:  Vladimir B Birman; Zhufeng Zhao; Lei Guo
Journal:  Org Lett       Date:  2007-03-01       Impact factor: 6.005
  4 in total
  2 in total

1.  Synthetic studies toward lapidilectine-type Kopsia alkaloids.

Authors:  Erica E Schultz; Brian G Pujanauski; Richmond Sarpong
Journal:  Org Lett       Date:  2012-01-03       Impact factor: 6.005

Review 2.  Application of Pauson-Khand reaction in the total synthesis of terpenes.

Authors:  Majid M Heravi; Leila Mohammadi
Journal:  RSC Adv       Date:  2021-11-29       Impact factor: 4.036
  2 in total

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