Stereoselective synthesis of the styryllactones, 7-epi-goniodiol and leiocarpin A, isolated from Goniothalamus leiocarpus

Tetrahedron Letters

Volumn 45, Issue 43, 2004, Pages 8111-8113

  Chen, Jian ^a   Lin, Guo Qiang ^a   Liu, Han Quan ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

7 epi Goniodiol; Epoxidation; Leiocarpin A; Styryllactones; Synthesized

Indexed keywords

7 EPIGONIODIOL; ANTIFUNGAL AGENT; ANTINEOPLASTIC AGENT; CINNAMYL ALCOHOL; EPOXIDE; LACTONE DERIVATIVE; LEIOCARPIN A; PALLADIUM; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ANNONACEAE; ARTICLE; CATALYSIS; CROSS COUPLING REACTION; DRUG ISOLATION; DRUG SYNTHESIS; EPOXIDATION; GONIOTHALAMUS LEIOCARPUS; STEREOCHEMISTRY;

GONIOTHALAMUS;

EID: 4644242031     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.132     Document Type: Article

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19. 5 N); δ 7.20-7.75 (m, 5H), 6.82 (ddd, J = 9.5 Hz, J = 5.9 Hz, J = 2.9 Hz), 5.95 (ddd, J = 9.5 Hz, J = 2.2 Hz, J = 1.1 Hz, 1H), 5.35 (d, J = 3.7 Hz, 1H), 4.80-5.80 (br s, 1H), 4.90 (dt, J = 10.8 Hz, J = 5.4 Hz, 1H), 4.30 (dd, J = 5.9 Hz, J = 3.8 Hz, 1H), 2.78 (m, 1H), 2.72 (m, 1H)
20. 5N): δ 4.8 (br s, 1H), 2.81 (dd, J = 5.2, 17.9, 1H), 2.9 (d, J = 19.5, 1H), 4.35 (br s, 1H), 4.41 (d, J = 8.8, 1H), 3.45 (d, J = 8.8, 1H), 2.11(br s, 1H), 7.25-7.43 (m, 5H)
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