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Volumn 59, Issue 35, 2003, Pages 6905-6919

Enantioselective synthesis of (-)-idiospermuline

Author keywords

Cyclotryptamine alkaloids; Dialkylation; Heck cyclization; Vicinal quaternary centers

Indexed keywords

CARBON; IDIOSPERMULINE; PYRROLIDINE DERIVATIVE; TARTARIC ACID; UNCLASSIFIED DRUG;

EID: 0042659376     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00855-X     Document Type: Article
Times cited : (65)

References (28)
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    • For examples of Stille cross-couplings at room temperature and the effect of tri-2-furylphosphine see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595. For the role of CuI see: (b) Farina V., Kapadia S., Krishnan B., Wang C., Liebeskind L.S. J. Org. Chem. 59:1994;5905-5911 (c) Liebeskind L.S., Fengl R.W. J. Org. Chem. 55:1990;5359-5364.
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    • For examples of Stille cross-couplings at room temperature and the effect of tri-2-furylphosphine see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595. For the role of CuI see: (b) Farina V., Kapadia S., Krishnan B., Wang C., Liebeskind L.S. J. Org. Chem. 59:1994;5905-5911 (c) Liebeskind L.S., Fengl R.W. J. Org. Chem. 55:1990;5359-5364.
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    • For examples of Stille cross-couplings at room temperature and the effect of tri-2-furylphosphine see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595. For the role of CuI see: (b) Farina V., Kapadia S., Krishnan B., Wang C., Liebeskind L.S. J. Org. Chem. 59:1994;5905-5911 (c) Liebeskind L.S., Fengl R.W. J. Org. Chem. 55:1990;5359-5364.
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    • For a recent review of the use of catalytic asymmetric intramolecular Heck reactions in the synthesis of natural products, see: in press
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    • Sodium (in ethanol) was the reductant employed in the first reported conversion of a 3-(2-aminoethyl)oxindole to a pyrrolidinoindoline:
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.