Sequential nucleophilic substitution on halogenated triazines, pyrimidines, and purines: A novel approach to cyclic peptidomimetics

Journal of Organic Chemistry

Volumn 66, Issue 2, 2001, Pages 507-513

  Scharn, D ^a   Germeroth, L ^b   Schneider Mergener, J ^b   Wenschuh, H ^b  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b Jerini Bio Tools GmbH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

2,4,6 TRICHLORO[1,3,5]TRIAZINE; 2,4,6 TRICHLOROPYRIMIDINE; 2,6,8 TRICHLORO 7 METHYLPURINE; 4,6 DICHLORO 5 NITROPYRIMIDINE; AMINO ACID; ARGON; AROMATIC COMPOUND; HALIDE; HETEROCYCLIC COMPOUND; MACROCYCLIC COMPOUND; OLIGOMER; PEPTIDE; PURINE DERIVATIVE; PYRIMIDINE DERIVATIVE; TRIAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; HALOGENATION; METHODOLOGY; SYNTHESIS;

AMINO ACID SEQUENCE; DIPEPTIDES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; OLIGOPEPTIDES; PEPTIDES, CYCLIC; PURINES; PYRIMIDINES; STRUCTURE-ACTIVITY RELATIONSHIP; TRIAZINES;

EID: 0035951563     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo005631q     Document Type: Article

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