Literature DB >> 17943211

Stereocontrolled synthesis of substituted N-arenesulfonyl azetidines from gamma-(phenylseleno)alkyl arylsulfonamides.

Marcello Tiecco1, Lorenzo Testaferri, Andrea Temperini, Raffaella Terlizzi, Luana Bagnoli, Francesca Marini, Claudio Santi.   

Abstract

Different synthetic methodologies for the stereocontrolled synthesis of substituted azetidines are reported. The approach utilizes an optimized oxidation reaction of gamma-(phenylseleno)alkyl arylsulfonamides, followed by the intramolecular substitution of the resulting phenylselenonyl group by the nitrogen atom.

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Year:  2007        PMID: 17943211     DOI: 10.1039/b712861d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Stereocontrolled total syntheses of isodomoic acids G and H via a unified strategy.

Authors:  Scott E Denmark; Jack Hung-Chang Liu; Joseck M Muhuhi
Journal:  J Org Chem       Date:  2010-12-01       Impact factor: 4.354

2.  Total syntheses of isodomoic acids G and H.

Authors:  Scott E Denmark; Jack Hung-Chang Liu; Joseck M Muhuhi
Journal:  J Am Chem Soc       Date:  2009-10-14       Impact factor: 15.419

3.  Magnesium bis(monoperoxyphthalate) hexahydrate as mild and efficient oxidant for the synthesis of selenones.

Authors:  Andrea Temperini; Massimo Curini; Ornelio Rosati; Lucio Minuti
Journal:  Beilstein J Org Chem       Date:  2014-06-02       Impact factor: 2.883

  3 in total

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