Highly Stereoselective Intermolecular Oxy-Michael Addition Reaction to α,β-Unsaturated Malonate Esters-Reference-Cited by-同舟云学术

Highly Stereoselective Intermolecular Oxy-Michael Addition Reaction to α,β-Unsaturated Malonate Esters

Published:2004-04-01 Issue:9 Volume:6 Page:1357-1360
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Buchanan David J.¹,Dixon Darren J.¹,Hernandez-Juan Felix A.¹

Affiliation:

1. Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol049820x

Reference12 articles.

1. Reviews: (a) Misra, M.; Luthra, R.; Singh, K. L.; Sushil, K. InComprehensiveNatural Products Chemistry; Barton, D. H. R., Nakunisha, K., Meth-Chon, O., Eds.; Pergamon: Oxford, UK, 1999; Vol. 4. p 25. (b) Staunton, J.; Wilkinson, B.Top. Curr. Chem.1998,195, 49.

2. Thiolate Bridged Nickel–Iron Complexes Containing both Iron(0) and Iron(II) Carbonyls

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