Literature DB >> 12182666

An effective procedure for the acylation of azaindoles at C-3.

Zhongxing Zhang1, Zhong Yang, Henry Wong, Juliang Zhu, Nicholas A Meanwell, John F Kadow, Tao Wang.   

Abstract

Conditions for attachment of acetyl chloride, benzoyl chloride, and chloromethyl oxalate to the 3-position of 4-, 5-, 6-, or 7-azaindoles were explored. Best results were achieved with an excess of AlCl(3) in CH(2)Cl(2) followed by the addition of an acyl chloride at room temperature.

Entities:  

Year:  2002        PMID: 12182666     DOI: 10.1021/jo020135i

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


  4 in total

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2.  Chemically Programmed Antibodies AS HIV-1 Attachment Inhibitors.

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Journal:  ACS Med Chem Lett       Date:  2013-05-09       Impact factor: 4.345

Review 3.  In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure-activity relationship and mechanistic insights.

Authors:  Dinesh Kumar; Pooja Sharma; Ramandeep Kaur; Maloba M M Lobe; Girish K Gupta; Fidele Ntie-Kang
Journal:  RSC Adv       Date:  2021-05-18       Impact factor: 4.036

Review 4.  Innovation in the discovery of the HIV-1 attachment inhibitor temsavir and its phosphonooxymethyl prodrug fostemsavir.

Authors:  Tao Wang; John F Kadow; Nicholas A Meanwell
Journal:  Med Chem Res       Date:  2021-09-28       Impact factor: 1.965

  4 in total

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