Literature DB >> 12945902

Intramolecular carbolithiation reactions for the preparation of 3-alkenylpyrrolidines.

Iain Coldham1, Kathy N Price, Richard E Rathmell.   

Abstract

Tin-lithium exchange allows the formation of alpha-amino-organolithium species that undergo anionic cyclization onto allylic ethers to give 3-alkenylpyrrolidines. The methodology has been applied to the synthesis of an advanced intermediate related to the natural product (-)-alpha-kainic acid.

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Year:  2003        PMID: 12945902     DOI: 10.1039/b303670g

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


  2 in total

1.  Diastereocontrolled construction of pactamycin's complex ureido triol functional array.

Authors:  Justin T Malinowski; Stefan J McCarver; Jeffrey S Johnson
Journal:  Org Lett       Date:  2012-05-22       Impact factor: 6.005

2.  Inter- and intramolecular enantioselective carbolithiation reactions.

Authors:  Asier Gómez-Sanjuan; Nuria Sotomayor; Esther Lete
Journal:  Beilstein J Org Chem       Date:  2013-02-13       Impact factor: 2.883

  2 in total

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