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Volumn 46, Issue 45, 2005, Pages 7781-7785

Efficient syntheses of new chiral peptidomimetic macrocycles through a configurationally driven preorganization

Author keywords

Chiral receptors; Macrocycles; Peptidomimetics; Preorganization; Supramolecular chemistry

Indexed keywords

IMINE; MACROCYCLIC COMPOUND;

EID: 26444436295     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.042     Document Type: Article
Times cited : (54)

References (48)
  • 28
    • 26444552881 scopus 로고    scopus 로고
    • note
    • 3. Addition of conc. HCl and evaporation of the solvents yielded the product as its hydrochloride salt.
  • 44
    • 26444483904 scopus 로고    scopus 로고
    • note
    • 13C NMR signals of the major species were unambiguously assigned by homonuclear (COSY, TOCSY, and NOESY) as well as heteronuclear (HSQC) correlation experiments.
  • 47
    • 26444600759 scopus 로고    scopus 로고
    • note
    • Initial molecular mechanics conformational search (MMFF94 force field) and AM1 semiempirical minimization were performed using PC Spartan program.
  • 48
    • 26444518743 scopus 로고    scopus 로고
    • note
    • 13C chemical shift of the NCH signal agree with a conjugated imine.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.