Literature DB >> 15179495

Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: radical ring-expansion to substituted tetrahydropyridines.

Peter G Turner1, Timothy J Donohoe, Rick P C Cousins.   

Abstract

Access to the synthetically important tetrahydropyridine motif has been achieved by radical rearrangement of pyrrolines obtained from the Birch reduction of electron-deficient pyrroles.

Entities:  

Year:  2004        PMID: 15179495     DOI: 10.1039/b404002c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Synthesis of Boc-protected bicycloproline.

Authors:  Sujeewa Ranatunga; Juan R Del Valle
Journal:  Tetrahedron Lett       Date:  2009-05-27       Impact factor: 2.415

  1 in total

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