Lewis acid-catalyzed one-pot crossed Prins cyclizations using allylchlorosilane as allylating agent

Tetrahedron Letters

Volumn 45, Issue 45, 2004, Pages 8387-8390

  Chan, Kok Ping ^a   Loh, Teck Peng ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

In(OTf) 3; InCl 3; Prins cyclization; Tetrahydropyran

Indexed keywords

ALDEHYDE DERIVATIVE; ALLYL COMPOUND; LEWIS ACID; SILANE DERIVATIVE; TETRAHYDROPYRAN DERIVATIVE;

ARTICLE; CATALYSIS; CYCLIZATION; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 5144229083     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.09.049     Document Type: Article

References (21)

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18. 4. The solvent was removed under reduced pressure to give the crude product, which was purified by flash column chromatography
19. 4. The solvent was removed under reduced pressure to give the crude product, which was purified by flash column chromatography
20. CCDC 246493 contains the supplementary crystallographic data for this paper. The data can be obtained free of charge via www.ccdc.cam.ac.uk/ data_request/cif, by e-mailing data_request@ccdc.cam.ac.uk, or by contacting The Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033
21. 3): δ 141.8, 128.5, 128.4, 125.9, 75.4, 55.8, 42.6, 37.4, 31.7