A novel intramolecular Diels-Alder approach to securinega alkaloids: Formal synthesis of securinine

Tetrahedron Letters

Volumn 41, Issue 31, 2000, Pages 5927-5930

  Honda, Toshio ^a   Namiki, Hidenori ^a   Kudoh, Mika ^a   Watanabe, Naofumi ^a   Nagase, Hiromasa ^a   Mizutani, Hirotake ^a  

^a HOSHI UNIVERSITY   (Japan)

Author keywords

Diels Alder reaction; Enol ester; GABA(A) receptor antagonist; Securinine

Indexed keywords

SECURININE;

ARTICLE; REACTION ANALYSIS; SYNTHESIS;

EID: 0034729972     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00976-X     Document Type: Article

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21. -3; 2111 reflections with 4.24°<2θ<120.02° were recorded on a four-circle diffractometer using graphite-monochromated Cu-Kα radiation. Of those, 1911 with I>3σ(I) were judged as observed. The structure was solved using MALTAN88. R=0.0385, Rw=0.0328.
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