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Volumn 69, Issue 26, 2013, Pages 5525-5536

Enantiospecific total synthesis of indole alkaloids (+)-eburnamonine, (-)-aspidospermidine and (-)-quebrachamine

Author keywords

Claisen rearrangement; Enantiospecific synthesis; Indole alkaloids; Total synthesis

Indexed keywords

ALCOHOL; ALDEHYDE; ALKALOID; ASPIDOSPERMIDINE; LACTIC ACID; QUEBRACHAMINE; UNCLASSIFIED DRUG; VINBURNINE;

EID: 84878227508     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.04.097     Document Type: Article
Times cited : (38)

References (98)
  • 16
    • 84860894461 scopus 로고    scopus 로고
    • Preliminary communication
    • Preliminary communication: K.R. Prasad, and J.E. Nidhiry Synlett 2012 1477
    • (2012) Synlett , pp. 1477
    • Prasad, K.R.1    Nidhiry, J.E.2
  • 86
    • 0032578671 scopus 로고    scopus 로고
    • See also Refs. 6b,e,g,i,k
    • A.G.H. Wee, and Q. Yu Tetrahedron 54 1998 13435 See also Refs. 6b,e,g,i,k
    • (1998) Tetrahedron , vol.54 , pp. 13435
    • Wee, A.G.H.1    Yu, Q.2
  • 97
    • 1642365909 scopus 로고    scopus 로고
    • For analysis purpose both the diastereomers were separated and the spectral and physical properties were compared with those reported in literature. See: H. Tanino, K. Fukuishi, M. Ushiyama, and K. Okada Tetrahedron 60 2004 3273
    • (2004) Tetrahedron , vol.60 , pp. 3273
    • Tanino, H.1    Fukuishi, K.2    Ushiyama, M.3    Okada, K.4
  • 98
    • 9844257155 scopus 로고
    • Although, better yields were reported for this transformation, we were able to obtain only 14% for two steps. We have not investigated the reaction either with other acids or under different conditions
    • Although, better yields were reported for this transformation, we were able to obtain only 14% for two steps. We have not investigated the reaction either with other acids or under different conditions G.F. Smith, and M.A. Wahid J. Chem. Soc. 1963 4002
    • (1963) J. Chem. Soc. , pp. 4002
    • Smith, G.F.1    Wahid, M.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.