A straightforward stereoselective synthesis of meso-, (S,S)- and (R,R)-2,6-diaminopimelic acids from cis-1,4-diacetoxycyclohept-2-ene

Bioorganic and Medicinal Chemistry Letters

Volumn 17, Issue 21, 2007, Pages 5894-5896

  Saito, Yukako ^a   Shinkai, Takumi ^a   Yoshimura, Yuichi ^a   Takahata, Hiroki ^a  

^a TOHOKU PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Amino acid; Antibacterial chemotherapy; Enzymatic desymmetriztion; Peptidoglycan

Indexed keywords

1,4 DIACETOXYCYCLOHEPT 2 ENE DERIVATIVE; 2,6 DIAMINOPIMELIC ACID DERIVATIVE; CYCLOHEPTENE; PIMELIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CHEMICAL REACTION KINETICS; CHIRALITY; DRUG SYNTHESIS; ENANTIOMER; ENZYME BINDING; NONHUMAN; OXIDATIVE STRESS; STEREOCHEMISTRY;

CYCLOHEPTANES; DIAMINOPIMELIC ACID; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 34548863663     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.07.106     Document Type: Article

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