Stereocontrolled formation of ketomethylene isosteres through tandem chain extension reactions

Journal of Organic Chemistry

Volumn 71, Issue 21, 2006, Pages 8140-8145

  Lin, Weimin ^a   Tryder, Nancy ^a   Su, Fan ^a   Zercher, Charles K ^a   Jasinski, Jerry P ^b   Butcher, Ray J ^c  

^a University of New Hampshire   (United States)

^b KEENE STATE COLLEGE   (United States)

^c HOWARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROPHILIC REAGENTS; KETOMETHYLENE ISOSTERES;

AMINO ACIDS; MOLECULAR STRUCTURE; SUBSTITUTION REACTIONS;

STEREOCHEMISTRY;

AMINO ACID DERIVATIVE; CARBENE; ESTER DERIVATIVE; KETOMETHYLENE ISOSTERE; KETONE DERIVATIVE; PEPTIDE; PROLINE; REAGENT; UNCLASSIFIED DRUG; ZINC; ZINC ENOLATE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; DIASTEREOISOMER; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; STEREOSPECIFICITY; STRUCTURE ANALYSIS; SYNTHESIS; TANDEM CHAIN EXTENSION REACTION;

KETONES;

EID: 33750001696     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061184o     Document Type: Article

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