Highly Diastereoselective Nitrone Cycloaddition onto a Chiral Ketene Equivalent: Asymmetric Synthesis of Cispentacin
Author:
Affiliation:
1. Department of Chemistry, University of Bristol, Cantock's Close, Bristol, and Celltech R+D Ltd, 216 Bath Road, Slough SL1 4EN, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol025665f
Reference32 articles.
1. Highly Endo- and Enantioselective Asymmetric Nitrone Cycloadditions Catalyzed by the Aqua Complex of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyl- oxazoline)−Nickel(II) Perchlorate. Transition Structure Based on Dramatic Effect of MS 4A on Selectivities
2. Asymmetric 1,3-Dipolar Cycloaddition Reactions
3. 1,3-Dipolar cycloaddition reactions of nitrones with alkyl vinyl ethers catalyzed by chiral oxazaborolidines
4. (1R,3R)-2-Methylene-1,3-dithiolane 1,3-dioxide: A highly reactive and selective chiral ketene equivalent.
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