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Volumn , Issue 7, 2011, Pages 1223-1226

Formal synthesis of galantinic acid by oxo-Diels-Alder methodology

Author keywords

Chromium; Cycloaddition; Natural products; Oxygen heterocycles

Indexed keywords


EID: 79951791596     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001296     Document Type: Article
Times cited : (8)

References (40)
  • 5
    • 79951791266 scopus 로고    scopus 로고
    • For the synthesis of anhydogalantinic acid 3
    • For the synthesis of anhydogalantinic acid 3, see
  • 35
    • 79951781418 scopus 로고    scopus 로고
    • For application of 10b in other reactions
    • For application of 10b in other reactions, see
  • 40
    • 79951789224 scopus 로고    scopus 로고
    • SES protection is sometimes hardly removable. In this case, the SES group seems to be easy to remove, which was demonstrated by deprotection of the amine group in compound 20, and by trapping the free amine as a Boc derivative. The conversion of 20 into the corresponding Boc derivative was accomplished in 39 yield in an non-optimized protocol
    • SES protection is sometimes hardly removable. In this case, the SES group seems to be easy to remove, which was demonstrated by deprotection of the amine group in compound 20, and by trapping the free amine as a Boc derivative. The conversion of 20 into the corresponding Boc derivative was accomplished in 39 yield in an non-optimized protocol.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.