Toward the total synthesis of maoecrystal V: An intramolecular Diels-Alder route to the maoecrystal V pentacyclic core with the appropriate relative stereochemistry Journal Article
| Authors: | Peng, F.; Danishefsky, S. J. |
| Article Title: | Toward the total synthesis of maoecrystal V: An intramolecular Diels-Alder route to the maoecrystal V pentacyclic core with the appropriate relative stereochemistry |
| Abstract: | A diastereoselective route to the maoecrystal V core compound (6) has been achieved. Key transformations include an intramolecular Diels-Alder cyclization and an exo-glycal epoxide rearrangement sequence. © 2010 Elsevier Ltd. All rights reserved. |
| Keywords: | unclassified drug; cyclization; diels alder reaction; reaction analysis; stereochemistry; alnus; diterpenoid; epoxide; maoecrystal 5 |
| Journal Title: | Tetrahedron Letters |
| Volume: | 52 |
| Issue: | 17 |
| ISSN: | 0040-4039 |
| Publisher: | Pergamon-Elsevier Science Ltd |
| Date Published: | 2011-04-27 |
| Start Page: | 2104 |
| End Page: | 2106 |
| Language: | English |
| DOI: | 10.1016/j.tetlet.2010.11.029 |
| PROVIDER: | scopus |
| PMCID: | PMC3079889 |
| PUBMED: | 21516211 |
| DOI/URL: | |
| Notes: | --- - "Export Date: 23 June 2011" - "CODEN: TELEA" - "Source: Scopus" |
