Literature DB >> 17914839

Selective defluorination approach to N-Cbz-3,3-difluoro-2-difluoromethylenepyrrolidine and its application to 3,3-difluoroproline dipeptide synthesis.

Yong Guo1, Kana Fujiwara, Hideki Amii, Kenji Uneyama.   

Abstract

Mg-promoted defluorination of N-(p-methoxyphenyl)bis(trifluoromethyl)imine 1 gave perfluoroenamine 2, which was readily transformed to N-Cbz-2-trifluoromethyl-3,3-difluoropyrrolidine 10. Chemoselective defluorination from the trifluoromethyl group of 10 by LHMDS-promoted dehydrofluorination in THF provided 3,3-difluoro-2-difluoromethylenepyrrolidine 11. The product 11 was converted to 3,3-difluoroproline dipeptides 16 upon treatment with aminoesters.

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Year:  2007        PMID: 17914839     DOI: 10.1021/jo070719q

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


  1 in total

1.  A mild and efficient synthesis of monofluorinated α-lactam pseudopeptides via a novel dehydrofluorination of Ugi products.

Authors:  Nianjin Liu; Song Cao; Jingjing Wu; Li Shen; Jinlong Yu; Jian Zhang; Hui Li; Xuhong Qian
Journal:  Mol Divers       Date:  2009-11-17       Impact factor: 2.943

  1 in total

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