Literature DB >> 15200320

Benzothiazines in synthesis. Toward the synthesis of pseudopteroxazole.

Michael Harmata1, Xuechuan Hong, Charles L Barnes.   

Abstract

[reaction: see text] The tricyclic benzothiazine 15 was prepared in a straightforward fashion via a completely stereoselective intramolecular Friedel-Crafts alkylation. This compound represents a potential precursor to the antitubercular agent, pseudopteroxazole. Its synthesis proceeded via a completely selective, intramolecular addition of a sulfoximine-stabilized carbanion to an alpha,beta-unsaturated ester, followed by functional group manipulations.

Entities:  

Year:  2004        PMID: 15200320     DOI: 10.1021/ol049334+

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


  4 in total

1.  Benzothiazines in organic synthesis. An approach to floresolide B.

Authors:  Yugang Chen; Michael Harmata
Journal:  Tetrahedron Lett       Date:  2011-08-10       Impact factor: 2.415

2.  1-Methyl-1H-2,1-benzothia-zin-4(3H)-one 2,2-dioxide.

Authors:  M Nawaz Tahir; Muhammad Shafiq; Islam Ullah Khan; Waseeq Ahmad Siddiqui; Muhammad Nadeem Arshad
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-02-06

3.  Benzothiazines in synthesis. Further studies of the intramolecular, stereoselective addition of sulfonimidoyl carbanions to alpha,beta-unsaturated functional groups.

Authors:  Michael Harmata; Kanok-on Rayanil; Vinson R Espejo; Charles L Barnes
Journal:  J Org Chem       Date:  2009-04-17       Impact factor: 4.354

4.  Benzothiazines in synthesis. A formal total synthesis of pseudopteroxazole.

Authors:  Michael Harmata; Zhengxin Cai; Yugang Chen
Journal:  J Org Chem       Date:  2009-08-07       Impact factor: 4.354

  4 in total

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