An ionic Diels-Alder route to cis-fused octalins containing an all-carbon quaternary stereocenter in an angular position Journal Article
| Authors: | Lee, J. H.; Kim, W. H.; Danishefsky, S. J. |
| Article Title: | An ionic Diels-Alder route to cis-fused octalins containing an all-carbon quaternary stereocenter in an angular position |
| Abstract: | We describe herein the development of efficient and stereoselective synthetic routes to a series of cis-octalins possessing an all-carbon quaternary center in an angular position. © 2009 Elsevier Ltd. All rights reserved. |
| Keywords: | controlled study; unclassified drug; hydrolysis; diels alder reaction; synthesis; stereochemistry; octalin derivative; carbon; alnus |
| Journal Title: | Tetrahedron Letters |
| Volume: | 51 |
| Issue: | 9 |
| ISSN: | 0040-4039 |
| Publisher: | Pergamon-Elsevier Science Ltd |
| Date Published: | 2010-03-03 |
| Start Page: | 1252 |
| End Page: | 1253 |
| Language: | English |
| DOI: | 10.1016/j.tetlet.2009.12.127 |
| PROVIDER: | scopus |
| PMCID: | PMC2822275 |
| PUBMED: | 20174450 |
| DOI/URL: | |
| Notes: | --- - "Cited By (since 1996): 1" - "Export Date: 20 April 2011" - "CODEN: TELEA" - "Source: Scopus" |
