π-Facial Diastereoselection in the 1,2-Addition of Allylmetal Reagents to 2-Methoxycyclohexanone and Tetrahydrofuranspiro-(2-cyclohexanone)-Reference-Cited by-同舟云学术

π-Facial Diastereoselection in the 1,2-Addition of Allylmetal Reagents to 2-Methoxycyclohexanone and Tetrahydrofuranspiro-(2-cyclohexanone)

Published:1996-01-01 Issue:8 Volume:118 Page:1917-1930
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Paquette Leo A.¹,Lobben Paul C.¹

Affiliation:

1. Contribution from the Evans Chemical Laboratories, The Ohio State University, Columbus, Ohio 43210

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9536835

Reference69 articles.

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2. (b) Houk, K. N.; Wu, Y.D. InStereochemistry of Organic and Bioorganic Transformations; Bartmann, W.; Sharpless, K. B., Eds., VCH: Weinheim, Germany, 1987; pp 247−260.

3. The Stereochemistry of Hydride Reductions

4. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

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