Literature DB >> 16557308

Natural cis-solamin is a mixture of two tetra-epimeric diastereoisomers: biosynthetic implications for Annonaceous acetogenins.

Yulai Hu1, Alex R L Cecil, Xavier Frank, Christophe Gleye, Bruno Figadère, Richard C D Brown.   

Abstract

The anti-tumour natural product cis-solamin has been shown to occur as a mixture two of tetra-epimeric diastereoisomers 1A and 1B, whereas solamin (6) was isolated as a single diastereoisomer; the biosyntheses of 1A/B and 6 are likely to involve enzyme-mediated cyclohydrations of the bis-epoxide acetogenins anti-diepomuricanin A2 and syn-diepomuricanin A1 respectively, where addition of water occurs regioselectively at either C15 or C20.

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Year:  2006        PMID: 16557308     DOI: 10.1039/b601943a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

Review 1.  Oxidative Cyclization in Natural Product Biosynthesis.

Authors:  Man-Cheng Tang; Yi Zou; Kenji Watanabe; Christopher T Walsh; Yi Tang
Journal:  Chem Rev       Date:  2016-12-12       Impact factor: 60.622

Review 2.  The direct oxidative diene cyclization and related reactions in natural product synthesis.

Authors:  Juliane Adrian; Leona J Gross; Christian B W Stark
Journal:  Beilstein J Org Chem       Date:  2016-09-30       Impact factor: 2.883

3.  Total synthesis of annonaceous acetogenins belonging to the non-adjacent bis-THF and non-adjacent THF-THP sub-classes.

Authors:  Ian B Spurr; Richard C D Brown
Journal:  Molecules       Date:  2010-01-21       Impact factor: 4.411

4.  Apolar Annonaceous acetogenins from the fruit pulp of Annona muricata.

Authors:  Alice Melot; Djibril Fall; Christophe Gleye; Pierre Champy
Journal:  Molecules       Date:  2009-11-02       Impact factor: 4.411

  4 in total

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