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-Reference-Cited by-同舟云学术

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

Published:1998-11-11 Issue:47 Volume:120 Page:12355-12356
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kanemasa Shuji¹,Oderaotoshi Yoji¹,Tanaka Junji¹,Wada Eiji¹

Affiliation:

1. Institute of Advanced Material Study, Kyushu University, Kasugakoen, Kasuga 816-8580, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja982254e

Reference22 articles.

1. Asymmetric 1,3-Dipolar Cycloaddition Reactions

2. (b) Tufariello, J. J.1,3-DipolarCycloaddition Chemistry; Padwa, A., Ed.; John Wiley & Sons: New York, 1984; Vol. 9, pp 83−168.

3. Control of regio-, diastereo-, and enantioselectivity in the [Ti(OTs)2(TADDOLato)]-catalyzed 1,3-dipolar cycloaddition reaction between 3-acryloyloxazolidin-2-one and nitrones

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