Role of the countercation in diastereoselective alkylations of pyramidalized bicyclic serine enolates. An easy approach to α-benzylserine

Journal of Organic Chemistry

Volumn 72, Issue 14, 2007, Pages 5399-5402

  Jiménez Osés, Gonzalo ^a   Aydillo, Carlos ^a   Busto, Jesús H ^a   Zurbano, María M ^a   Peregrina, Jesús M ^a   Avenoza, Alberto ^a  

^a UNIVERSITY OF LA RIOJA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

BENZYLSERINE; BUILDING BLOCKS; CONFIGURATION; COUNTERCATIONS;

ALKYLATION; CHIRALITY; DERIVATIVES; HYDROLYSIS; POSITIVE IONS; STEREOSELECTIVITY;

AMINO ACIDS;

ALPHA BENZYLSERINE; BICYCLO COMPOUND; CATION; LITHIUM; SERINE DERIVATIVE; SERINE ENOLATE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; BINDING COMPETITION; CHIRALITY; DIASTEREOISOMER; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY ANALYSIS;

ALKYLATION; BENZYL COMPOUNDS; CYCLIZATION; MODELS, MOLECULAR; MOLECULAR STRUCTURE; SERINE; STEREOISOMERISM;

EID: 34447334168     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070656b     Document Type: Article

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