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Volumn 4, Issue 25, 2002, Pages 4455-4458

Synthesis of the Unnatural Amino Acid AGDHE, a Constituent of the Cyclic Depsipeptides Callipeltins A and D

Author keywords

[No Author keywords available]

Indexed keywords

4 AMIDO 7 GUANIDINO 2,3 DIHYDROXYHEPTANOIC ACID; 4-AMIDO-7-GUANIDINO-2,3-DIHYDROXYHEPTANOIC ACID; AMINO ACID; CALLIPELTIN A; CALLIPELTIN D; CYCLOPEPTIDE; DEPSIPEPTIDE; GUANIDINE DERIVATIVE; HEPTANOIC ACID DERIVATIVE;

EID: 0037069729     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0269852     Document Type: Article
Times cited : (44)

References (21)
  • 12
    • 0442266125 scopus 로고    scopus 로고
    • note
    • 13C NMR) and analytical data in accord with the assigned structures.
  • 15
    • 0442266127 scopus 로고    scopus 로고
    • 1H NMR indicated >60:1 ratio of Z/E alkenes
    • 1H NMR indicated >60:1 ratio of Z/E alkenes.
  • 19
    • 0442264542 scopus 로고    scopus 로고
    • note
    • The configuration of the dihydroxylation products (12a and 12b) was determined by conversion of the aminodiol to an oxazolidinone and examination of the coupling constant between H-3 and H-4: (Matrix Presented)
  • 21
    • 0442266128 scopus 로고    scopus 로고
    • note
    • Further confirmation of the (2S,3R,4R) stereochemical assignment was obtained from the observation of NOE enhancements in the lactam derived from 11a: (Matrix Presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.