Scope of stereoselective Mn-mediated radical addition to chiral hydrazones and application in a formal synthesis of quinine

Journal of Organic Chemistry

Volumn 77, Issue 7, 2012, Pages 3159-3180

  Friestad, Gregory K ^a   Ji, An ^a   Baltrusaitis, Jonas ^a   Korapala, Chandra Sekhar ^a   Qin, Jun ^a  

^a University of Iowa   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL IODIDES; B3LYP/6-31G; C-C BONDS; CHIRAL AMINES; CYCLIZATIONS; FORMAL SYNTHESIS; HYDRAZONES; N-ACYLHYDRAZONES; RADICAL ACCEPTORS; RADICAL ADDITION; RADICAL PRECURSOR; RING SYSTEMS; STEREO-SELECTIVE; STEREOCHEMICAL CONTROL; STEREOGENIC CENTERS; SYNTHETIC APPROACH; TRANSITION STATE;

CYCLIZATION; OLEFINS; ORGANIC COMPOUNDS;

MANGANESE;

HYDRAZONE DERIVATIVE; MANGANESE; QUINCORINE; QUININE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL BOND; CHIRALITY; CYCLIZATION; STEREOCHEMISTRY; SYNTHESIS;

HYDRAZONES; MANGANESE; MOLECULAR STRUCTURE; QUININE; STEREOISOMERISM;

EID: 84859581047     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo2026349     Document Type: Article

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