Literature DB >> 19606883

Synthesis of plakortethers F and G.

Jinu P John1, Joshua Jost, Alexei V Novikov.   

Abstract

Synthesis of plakortethers F and G has been performed by taking advantage of the symmetry in the structure. The structures of the prepared compounds have been confirmed by COSY, 1D NOE, and chemical transformation studies. The synthetic plakortether F was found to match the natural product by all physical data. The synthetic plakortether G exhibited several disagreements in (13)C NMR data with the reported values. However, on the basis of an extremely close match in appearance of its (1)H NMR spectrum to the obtained (1)H NMR spectrum of the natural product, as well as matching optical rotations, the two compounds are believed to be identical.

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Year:  2009        PMID: 19606883     DOI: 10.1021/jo901203s

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Samarium iodide-mediated Reformatsky reactions for the stereoselective preparation of β-hydroxy-γ-amino acids: synthesis of isostatine and dolaisoleucine.

Authors:  Christopher G Nelson; Terrence R Burke
Journal:  J Org Chem       Date:  2011-12-14       Impact factor: 4.354

2.  Woodylides A-C, new cytotoxic linear polyketides from the South China Sea sponge Plakortis simplex.

Authors:  Hao-Bing Yu; Xiang-Fang Liu; Ying Xu; Jian-Hong Gan; Wei-Hua Jiao; Yang Shen; Hou-Wen Lin
Journal:  Mar Drugs       Date:  2012-05-07       Impact factor: 6.085

  2 in total

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