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https://doi.org/10.1016/j.tetlet.2004.09.049
| Title: | Lewis acid-catalyzed one-pot crossed Prins cyclizations using allylchlorosilane as allylating agent | Authors: | Chan, K.-P. Loh, T.-P. |
Keywords: | In(OTf) 3 InCl 3 Prins cyclization Tetrahydropyran |
Issue Date: | 1-Nov-2004 | Citation: | Chan, K.-P., Loh, T.-P. (2004-11-01). Lewis acid-catalyzed one-pot crossed Prins cyclizations using allylchlorosilane as allylating agent. Tetrahedron Letters 45 (45) : 8387-8390. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2004.09.049 | Abstract: | A one-pot multi-component Lewis acid-catalyzed Prins cyclization was developed with high yield and selectivity. The crossed 2,4,6-trisubstituted tetrahydropyran products were formed with high stereoselectivity. This catalytic method could also be used with α,β-unsaturated aldehydes affording moderate yields of products. A one-pot multi-component Lewis acid-catalyzed Prins cyclization was developed with high yield and selectivity. The crossed 2,4,6-trisubstituted tetrahydropyran products were formed with high stereoselectivity. This catalytic method could also be used with α,β-unsaturated aldehydes affording moderate yields of products. © 2004 Elsevier Ltd. All rights reserved. | Source Title: | Tetrahedron Letters | URI: | http://scholarbank.nus.edu.sg/handle/10635/76440 | ISSN: | 00404039 | DOI: | 10.1016/j.tetlet.2004.09.049 |
| Appears in Collections: | Staff Publications |
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