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Sequential 1,4- and 1,2-addition reactions to α,β-unsaturated N-acyliminium ions: a new strategy for the synthesis of spiro and bridged heterocycles

Journal Article


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Abstract


  • Novel bicyclic and tetracyclic spirocycles and tricyclic bridged heterocyclic systems can be readily prepared from sequential 1,4- and 1,2-addition reactions of latent bis-nucleophiles to α,β-unsaturated N-acyliminium ions. © 2013 American Chemical Society.

UOW Authors


Publication Date


  • 2013

Citation


  • Yazici, A. & Pyne, S. G. (2013). Sequential 1,4- and 1,2-addition reactions to α,β-unsaturated N-acyliminium ions: a new strategy for the synthesis of spiro and bridged heterocycles. Organic Letters, 15 (22), 5878-5881.

Scopus Eid


  • 2-s2.0-84887902706

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=2250&context=smhpapers

Ro Metadata Url


  • http://ro.uow.edu.au/smhpapers/1232

Has Global Citation Frequency


Number Of Pages


  • 3

Start Page


  • 5878

End Page


  • 5881

Volume


  • 15

Issue


  • 22

Place Of Publication


  • United States

Abstract


  • Novel bicyclic and tetracyclic spirocycles and tricyclic bridged heterocyclic systems can be readily prepared from sequential 1,4- and 1,2-addition reactions of latent bis-nucleophiles to α,β-unsaturated N-acyliminium ions. © 2013 American Chemical Society.

UOW Authors


Publication Date


  • 2013

Citation


  • Yazici, A. & Pyne, S. G. (2013). Sequential 1,4- and 1,2-addition reactions to α,β-unsaturated N-acyliminium ions: a new strategy for the synthesis of spiro and bridged heterocycles. Organic Letters, 15 (22), 5878-5881.

Scopus Eid


  • 2-s2.0-84887902706

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=2250&context=smhpapers

Ro Metadata Url


  • http://ro.uow.edu.au/smhpapers/1232

Has Global Citation Frequency


Number Of Pages


  • 3

Start Page


  • 5878

End Page


  • 5881

Volume


  • 15

Issue


  • 22

Place Of Publication


  • United States