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Volumn , Issue 17, 2005, Pages 2599-2602

Model studies towards the total synthesis of GKK1032s, novel antibiotic anti-tumor agents: Enantioselective synthesis of the alkyl aryl ether portion of GKK1032s

Author keywords

Anti tumor agent; Antibiotic; GKK1032s; Mitsunobu reaction; Natural products synthesis; Saegusa oxidation

Indexed keywords

ALKYL ARYL ETHER; ANTIBIOTIC AGENT; ANTINEOPLASTIC AGENT; BENZENE; GKK 1032; INDANONE DERIVATIVE; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 27444431675     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-917112     Document Type: Article
Times cited : (27)

References (27)
  • 23
    • 27444440426 scopus 로고    scopus 로고
    • note
    • +]: 192.0786; found: 192.0790.
  • 24
    • 27444440759 scopus 로고    scopus 로고
    • note
    • This remarkable stereoselectivity can be rationalized by the consideration that the hydride attack occurred exclusively from α-face of the carbonyl group under an influence of stereoelectronic effect, which may involve the so-called 'product development control'.
  • 25
    • 27444432110 scopus 로고    scopus 로고
    • note
    • 1H NMR (500 MHz) spectroscopy.
  • 27
    • 27444447780 scopus 로고    scopus 로고
    • note
    • +]: 194.1671; found: 194.1667.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.