Literature DB >> 11348209

Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis.

P Wipf1, J L Methot.   

Abstract

[Reaction in text]The indole-bisoxazole fragment of diazonamide A was prepared by a Chan-type rearrangement of a tertiary amide. This approach represents a remarkably direct strategy for polyoxazole synthesis.

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Year:  2001        PMID： 11348209     DOI： 10.1021/ol0157196

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


  4 in total

1.  An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary center.

Authors:  Chi-Ming Cheung; Frederick W Goldberg; Philip Magnus; Claire J Russell; Rachel Turnbull; Vince Lynch
Journal:  J Am Chem Soc       Date:  2007-09-19       Impact factor: 15.419

2.  Ugi/Robinson-Gabriel reactions directed toward the synthesis of 2,4,5-trisubstituted oxazoles.

Authors:  Arthur Y Shaw; Zhigang Xu; Christopher Hulme
Journal:  Tetrahedron Lett       Date:  2012-02-13       Impact factor: 2.415

3.  Synthesis of monoalkylidene diketopiperazines and application to the synthesis of barettin.

Authors:  Elizabeth W Kelley; Skylar G Norman; Jonathan R Scheerer
Journal:  Org Biomol Chem       Date:  2017-10-18       Impact factor: 3.876

4.  Retracted Article: Metal-free [2+2+1] cycloaddition polymerization of alkynes, nitriles, and oxygen atoms to functional polyoxazoles.

Authors:  Lichao Dong; Tian Lan; Yin Liang; Shifeng Guo; Hao Zhang
Journal:  RSC Adv       Date:  2020-06-25       Impact factor: 4.036
  4 in total

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