Abstract
An one-pot TiCl4 initiated assemblage of polyfunctional compounds via a sequential coupling of p-TolSCl, 1-methoxycycloalkene, methyl vinyl ether and Sn-or Si-capped carbon nucleophile is shown to proceed with high diastereoselectivity at all newly created chiral centres.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 24-25 |
| Number of pages | 2 |
| Journal | Mendeleev Communications |
| Volume | 9 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1999 |
Bibliographical note
Funding Information:This work was supported by the National Science Foundation (grant no. 8921358), the U.S. Civilian Research and Development Foundation (award no. RC2-141) and the Russian Foundation for Basic Research (grant no. 98-03-32970a).
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
Fingerprint
Dive into the research topics of 'Highly diastereoselective one-pot four-component coupling of p-TolSCl, 1-methoxycycloalkene, methyl vinyl ether and a carbon nucleophile leading to the synthesis of polyfunctional compounds'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS