Literature DB >> 11975600

Studies on the biosynthesis of phomoidride B (CP-263,114): evidence for a decarboxylative homodimerization pathway.

Gary A Sulikowski1, Fabio Agnelli, Paul Spencer, John M Koomen, David H Russell.   

Abstract

[reaction: see text]. Feeding experiments using a deuterium labeled C16 maleic anhydride and whole cell culture of ATCC 74256 led to the isolation of phomoidride B with deuterium incorporation at C(7) and C(19) as determined by 2H NMR and electrospray mass spectrometry. This result is in accord with a decarboxylative homodimerization of the C16 maleic anhydride as a key biosynthetic step leading to phomoidride B.

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Year:  2002        PMID: 11975600     DOI: 10.1021/ol025594k

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


  2 in total

1.  A strategy for complex dimer formation when biomimicry fails: total synthesis of ten coccinellid alkaloids.

Authors:  Trevor C Sherwood; Adam H Trotta; Scott A Snyder
Journal:  J Am Chem Soc       Date:  2014-06-24       Impact factor: 15.419

2.  Novel nonadride, heptadride and maleic acid metabolites from the byssochlamic acid producer Byssochlamys fulva IMI 40021 - an insight into the biosynthesis of maleidrides.

Authors:  Agnieszka J Szwalbe; Katherine Williams; Daniel E O'Flynn; Andrew M Bailey; Nicholas P Mulholland; Jason L Vincent; Christine L Willis; Russell J Cox; Thomas J Simpson
Journal:  Chem Commun (Camb)       Date:  2015-12-14       Impact factor: 6.222

  2 in total

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