Literature DB >> 12098253

Total synthesis of caerulomycin C via the halogen dance reaction.

Tarek Sammakia1, Eric L Stangeland, Mark C Whitcomb.   

Abstract

[reaction: see text] The total synthesis of caerulomycin C is described. Key steps in this synthesis utilize 1,2-, 1,3-, and 1,4-halogen dance reactions for the functionalization of the pyridine ring.

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Year:  2002        PMID： 12098253     DOI： 10.1021/ol026135m

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


  3 in total

1.  An Efficient Synthesis of Arylated Pyridines from Conjugated Acetylenes and Substituted Benzylamines Catalyzed by Base.

Authors:  Mengping Guo; Bo Chen; Qiming Zhu; Hua Jin; Qiuling Peng; Yanping Kang
Journal:  Molecules       Date:  2017-07-31       Impact factor: 4.411

2.  Base-catalyzed aryl halide isomerization enables the 4-selective substitution of 3-bromopyridines.

Authors:  Thomas R Puleo; Jeffrey S Bandar
Journal:  Chem Sci       Date:  2020-09-09       Impact factor: 9.825

3.  Ester dance reaction on the aromatic ring.

Authors:  Kaoru Matsushita; Ryosuke Takise; Kei Muto; Junichiro Yamaguchi
Journal:  Sci Adv       Date:  2020-07-08       Impact factor: 14.136
  3 in total

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