Literature DB >> 20450183

Syntheses of optically pure conduramines via the strategy of hetero Diels-Alder reaction of masked o-benzoquinones with homochiral nitroso dienophiles.

Ping-Hsun Lu1, Ching-Shun Yang, Badugu Devendar, Chun-Chen Liao.   

Abstract

Highly stereoselective hetero Diels-Alder reactions of masked o-benzoquinones (MOBs) with homochiral nitroso dienophiles are described along with their application in the syntheses of (+)-ent-conduramine F-1, (+)-conduramine E-1, (-)-conduramine A-1, (+)-conduramine A-1 tetraacetate, and (-)-ent-conduramine A-1 tetraacetate.

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Year:  2010        PMID: 20450183     DOI: 10.1021/ol100840n

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


  4 in total

1.  Highly Functionalized Tricyclic Oxazinanones via Pairwise Oxidative Dearomatization and N-Hydroxycarbamate Dehydrogenation: Molecular Diversity Inspired by Tetrodotoxin.

Authors:  Steffen N Good; Robert J Sharpe; Jeffrey S Johnson
Journal:  J Am Chem Soc       Date:  2017-08-30       Impact factor: 15.419

2.  Asymmetric stereodivergent strategy towards aminocyclitols.

Authors:  Barry M Trost; Sushant Malhotra
Journal:  Chemistry       Date:  2014-05-28       Impact factor: 5.236

Review 3.  Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes.

Authors:  Lucie Brulíková; Aidan Harrison; Marvin J Miller; Jan Hlaváč
Journal:  Beilstein J Org Chem       Date:  2016-09-01       Impact factor: 2.883

4.  Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents.

Authors:  Hisato Shimizu; Akira Yoshimura; Keiichi Noguchi; Victor N Nemykin; Viktor V Zhdankin; Akio Saito
Journal:  Beilstein J Org Chem       Date:  2018-02-28       Impact factor: 2.883

  4 in total

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