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Volumn 55, Issue 36, 1999, Pages 10989-11000

A formal synthesis of optically active clavicipitic acids, unusual azepinoindole-type ergot alkaloids

Author keywords

[No Author keywords available]

Indexed keywords

1 TERT BUTOXYCARBONYL 3 CHLOROMETHYL 4 [3 METHOXY 3 METHYL 1 BUTENYL]INDOLE; 2,5 DIHYDRO 2 ISOPROPYL 3,6 DIMETHOXYPYRAZINE; AZEPINOINDOLE; CLAVICIPITIC ACID; ERGOT ALKALOID; UNCLASSIFIED DRUG;

EID: 0033520222     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00626-2     Document Type: Article
Times cited : (36)

References (29)
  • 19
    • 0030047733 scopus 로고    scopus 로고
    • For the synthesis of benzyl chlorides from N,N-dialkyllbenzylamines, see: a) Matulenko, M. A.; Meyers, A. I. J. Org. Chem. 1996, 61, 573.
    • (1996) J. Org. Chem. , vol.61 , pp. 573
    • Matulenko, M.A.1    Meyers, A.I.2
  • 22
    • 0009567711 scopus 로고    scopus 로고
    • Recently, some examples of unusually poor diastereoselectivity in the alkylation of Scöllkopf's bislactim ethers depending on the structures of alkylating agents have been reported
    • Recently, some examples of unusually poor diastereoselectivity in the alkylation of Scöllkopf's bislactim ethers depending on the structures of alkylating agents have been reported.
  • 29
    • 0009580309 scopus 로고    scopus 로고
    • The authors are grateful to Professor Yasuoki Murakami (Toho University) for his kind correspondence concerning HPLC conditions to determine enantiomeric excess of clavicipitic acid derivatives
    • The authors are grateful to Professor Yasuoki Murakami (Toho University) for his kind correspondence concerning HPLC conditions to determine enantiomeric excess of clavicipitic acid derivatives.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.