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Volumn 65, Issue 21, 2000, Pages 6868-6875

How borane reagents based on α-pinene control stereoselectivity in the reductions of carbonyl groups with different stereogenic elements. 3. The effect of the relative size and conformation of the carbonyl substituents on the stereoselectivity of the Ipc2BCl, Eap2BCl, B-t-Bu-IpcBCl, and B-t-Bu-EapBCl reagents. A semiempirical study

(1) Rogic, M M a

a Molecular Modeling Research Studio (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BENZALDEHYDE; BORANE DERIVATIVE; CARBONYL DERIVATIVE; KETONE; PINENE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CONFORMATION; ENERGY; MOLECULAR INTERACTION; STEREOCHEMISTRY;

EID: 0034693125 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo000367m Document Type: Article

Times cited : (6)

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