Literature DB >> 18979485

An efficient substrate-controlled approach towards hypoestoxide, a member of a family of diterpenoid natural products with an inside-out [9.3.1]bicyclic core.

Nicholas A McGrath1, Christopher A Lee, Hiroshi Araki, Matthew Brichacek, Jon T Njardarson.   

Abstract

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Year:  2008        PMID： 18979485     DOI： 10.1002/anie.200804237

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


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  4 in total

1.  Evolution of an oxidative dearomatization enabled total synthesis of vinigrol.

Authors:  Qingliang Yang; Cristian Draghici; Jon T Njardarson; Fang Li; Brandon R Smith; Pradipta Das
Journal:  Org Biomol Chem       Date:  2014-01-14       Impact factor: 3.876

2.  Syntheses and structural confirmations of members of a heterocycle-containing family of labdane diterpenoids.

Authors:  Daniel J Mack; Jon T Njardarson
Journal:  Angew Chem Int Ed Engl       Date:  2012-12-17       Impact factor: 15.336

3.  Asymmetric approach toward chiral cyclohex-2-enones from anisoles via an enantioselective isomerization by a new chiral diamine catalyst.

Authors:  Jung Hwa Lee; Li Deng
Journal:  J Am Chem Soc       Date:  2012-10-22       Impact factor: 15.419

4.  Evolution of a Unified Strategy for Complex Sesterterpenoids: Progress toward Astellatol and the Total Synthesis of (-)-Nitidasin.

Authors:  Daniel T Hog; Florian M E Huber; Gonzalo Jiménez-Osés; Peter Mayer; Kendall N Houk; Dirk Trauner
Journal:  Chemistry       Date:  2015-08-20       Impact factor: 5.236
  4 in total

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