Literature DB >> 9548830

Tribenzylbutyrolactones and Dibenzyldiphenyl-4,5,6,7-tetrahydrobenzofuranones from Kyrtuthrix maculans

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Abstract

Ten novel compounds, maculalactones B-K (2-11), have been isolated from the marine cyanobacterium Kyrtuthrix maculans. Their structures, which involve either three benzyl groups substituted on a butyrolactone ring or two benzyl and two phenyl groups substituted on a 4,5,6,7-tetrahydrobenzofuranone nucleus, were determined by 2D NMR spectroscopy. Some speculation is made concerning the biogenesis of these two novel classes of natural products.

Entities:  

Year:  1998        PMID: 9548830     DOI: 10.1021/np970322p

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  2 in total

1.  Synthesis of Unusually Strained Spiro Ring Systems and Their Exploits in Synthesis.

Authors:  Richard J Duffy; Kay A Morris; Daniel Romo
Journal:  Tetrahedron       Date:  2009-09-01       Impact factor: 2.457

2.  Asymmetric synthesis, structure, and reactivity of unexpectedly stable spiroepoxy-beta-lactones including facile conversion to tetronic acids: application to (+)-maculalactone A.

Authors:  Richard J Duffy; Kay A Morris; Ravikrishna Vallakati; Wei Zhang; Daniel Romo
Journal:  J Org Chem       Date:  2009-07-03       Impact factor: 4.354

  2 in total

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