Asymmetric synthesis of α,α-disubstituted α-amino acids by diastereoselective alkylation of camphor-based tricyclic iminolactone

Journal of Organic Chemistry

Volumn 71, Issue 12, 2006, Pages 4364-4373

  Xu, Peng Fei ^a   Li, Shuo ^a   Lu, Ta Jung ^b   Wu, Chen Chang ^b   Fan, Botao ^c   Golfis, Georgia ^c  

^a LANZHOU UNIVERSITY   (Taiwan)

^b NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

^c UNIVERSITÉ PARIS DIDEROT   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CAMPHOR; DIASTEREOSELECTIVE ALKYLATION; DISUBSTITUTED PRODUCTS; TRICYCLIC IMINOLACTONE;

HYDROLYSIS; MOLECULAR ORIENTATION; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

AMINO ACIDS;

1,11,11 TRIMETHYL 3 OXA 6 AZATRICYCLO[6.2.1.0]UNDEC 6 EN 4 ONE; 2 METHYLPHENYLALANINE; 2 PROPENYLPHENYLALANINE; 8,11,11 TRIMETHYL 3 OXA 6 AZATRICYCLO[6.2.1.0]UNDEC 6 EN 4 ONE; ALPHA AMINO ACID; CAMPHOR; CAMPHORQUINONE; LACTONE DERIVATIVE; TRICYCLIC IMINOLACTONE; UNCLASSIFIED DRUG;

ALKYLATION; AMINO ACID SYNTHESIS; ARTICLE; ASYMMETRIC SYNTHESIS; CALCULATION; CHIRALITY; DIASTEREOISOMER; ENANTIOMER; HYDROLYSIS; PRODUCT YIELD; SEMIEMPIRICAL CALCULATION; STEREOCHEMISTRY;

ALKYLATION; AMINO ACIDS; CAMPHOR; HETEROCYCLIC COMPOUNDS, 3-RING; IMINES; LACTONES; MODELS, MOLECULAR; STEREOISOMERISM;

EID: 33744905212     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052435g     Document Type: Article

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