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Volumn 66, Issue 10, 2001, Pages 3538-3547

Entry to new conformationally constrained amino acids. First synthesis of 3-unsubstituted 4-alkyl-4-carboxy-2-azetidinone derivatives via an intramolecular Nα-Cα-cyclization strategy

(5) Gerona Navarro, G a Bonache, M A a Herranz, R a Garcia Lopez M T a Gonzalez Muniz R a

a INSTITUTO DE QUÍMICA MÉDICA (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIZATION REACTION;

ALKYLATION; SYNTHESIS (CHEMICAL);

AMINO ACIDS;

4 CARBOXY 2 AZETIDINONE DERIVATIVE; AMINO ACID DERIVATIVE; AZETIDINONE DERIVATIVE; BETA LACTAM DERIVATIVE; LEUCINE; PHENYLALANINE DERIVATIVE; PIPERAZINEDIONE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CYCLIZATION; MOLECULAR DYNAMICS; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

AMINO ACIDS; AZETIDINES; CYCLIZATION; LACTAMS; MOLECULAR CONFORMATION;

EID: 0035906484 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo015559b Document Type: Article

Times cited : (80)

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