An approach to the synthesis of tricholomalide A: an effective means for achieving homo-Robinson annulation Journal Article
| Authors: | Min, S. J.; Danishefsky, S. J. |
| Article Title: | An approach to the synthesis of tricholomalide A: an effective means for achieving homo-Robinson annulation |
| Abstract: | A procedure has been developed for the construction of 7,5-fused ring systems through the ring expansion of silyl enol ethers. This method has been applied to the synthesis of an intermediate en route to the natural product, tricholomalide A. © 2008 Elsevier Ltd. All rights reserved. |
| Keywords: | chemical structure; natural product; technique; chemical reaction; synthesis; stereochemistry; tricholomalide a; conjugation; cyclopropanation; annulation reaction; lactone; robinson annulation |
| Journal Title: | Tetrahedron Letters |
| Volume: | 49 |
| Issue: | 21 |
| ISSN: | 0040-4039 |
| Publisher: | Pergamon-Elsevier Science Ltd |
| Date Published: | 2008-05-19 |
| Start Page: | 3496 |
| End Page: | 3499 |
| Language: | English |
| DOI: | 10.1016/j.tetlet.2008.03.101 |
| PROVIDER: | scopus |
| PMCID: | PMC2430101 |
| PUBMED: | 19461989 |
| DOI/URL: | |
| Notes: | --- - "Cited By (since 1996): 2" - "Export Date: 17 November 2011" - "CODEN: TELEA" - "Source: Scopus" |
