4.5 Article

Diastereoselective [4+3] cycloadditions of enantiopure nitrogen-stabilized oxyallyl cations

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2006, Issue 16, Pages 3667-3680

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200600226

Keywords

cycloaddition; diastereoselectivity; chiral auxiliaries; oxyallyl cations

Ask authors/readers for more resources

Diastereoselective trapping of chiral enantiopure oxyallyl cations by common dienes is reported. Excellent diastereoselectivities were obtained and depending on which auxiliary was used cycloadditions proceeded through a chelated or non-chelated pathway. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 694 1 Weinheim, Germany, 2006)

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available