Literature DB >> 16268611

Polyfunctional tetrahydropyrido[2,3-b]pyrazine scaffolds from 4-phenylsulfonyl tetrafluoropyridine.

Aurelie Baron1, Graham Sandford, Rachel Slater, Dmitry S Yufit, Judith A K Howard, Antonio Vong.   

Abstract

[Reaction: see text]. Polyfunctional tetrahydropyrido[2,3-b]pyrazine scaffolds can be synthesized by sequential reaction of pentafluoropyridine with sodium phenylsulfinate and an appropriate diamine. The polyfunctionality possessed by the difluorinated tetrahydropyrido[2,3-b]pyrazine scaffolds was demonstrated in selected model reactions with nucleophiles to give access to various polysubstituted [6,6]-ring fused systems.

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Year:  2005        PMID: 16268611     DOI: 10.1021/jo051453v

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


  2 in total

1.  9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine.

Authors:  Graham Pattison; Graham Sandford; Dmitrii S Yufit; Judith A K Howard; John A Christopher; David D Miller
Journal:  Beilstein J Org Chem       Date:  2010-05-06       Impact factor: 2.883

2.  Perhalogenated pyrimidine scaffolds. Reactions of 5-chloro-2,4,6-trifluoropyrimidine with nitrogen centred nucleophiles.

Authors:  Emma L Parks; Graham Sandford; John A Christopher; David D Miller
Journal:  Beilstein J Org Chem       Date:  2008-07-01       Impact factor: 2.883

  2 in total

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