Literature DB >> 11440591

Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation.

N Hayashi1, Y Kobayashi, Y Kishi.   

Abstract

[structure: see text] Three additional NMR databases, 1-3, in a chiral solvent are presented. The C.21-C.38 portion of oasomycin A is used to demonstrate the scope and limitation of the universal NMR database approach in a chiral solvent for assignment of relative and absolute stereochemistry without degradation and/or derivatization.

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Year:  2001        PMID: 11440591     DOI: 10.1021/ol010109r

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


  4 in total

1.  Gargantulide A, a complex 52-membered macrolactone showing antibacterial activity from Streptomyces sp.

Authors:  Jung-Rae Rho; Gurusamy Subramaniam; Hyukjae Choi; Eun-Hee Kim; Sok Peng Ng; K Yoganathan; Siewbee Ng; Antony D Buss; Mark S Butler; William H Gerwick
Journal:  Org Lett       Date:  2015-02-27       Impact factor: 6.005

2.  Total Synthesis of Mycolactones A and B.

Authors:  Fengbin Song; Steve Fidanze; Andrew B Benowitz; Yoshito Kishi
Journal:  Tetrahedron       Date:  2007-06-25       Impact factor: 2.457

3.  A synthetic entry to pladienolide B and FD-895.

Authors:  Alexander L Mandel; Brian D Jones; James J La Clair; Michael D Burkart
Journal:  Bioorg Med Chem Lett       Date:  2007-07-07       Impact factor: 2.823

4.  INTEGRATED APPROACHES TO THE CONFIGURATIONAL ASSIGNMENT OF MARINE NATURAL PRODUCTS.

Authors:  Tadeusz F Molinski; Brandon I Morinaka
Journal:  Tetrahedron       Date:  2012-11-18       Impact factor: 2.457

  4 in total

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