A facile and efficient asymmetric synthesis of (+)-salsolidine
β Scribed by Daisuke Taniyama; Masayoshi Hasegawa; Kiyoshi Tomioka
- Book ID
- 104210509
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 222 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A three-key step methodology involving a highly selective asymmetric addition of an organolithium reagent to an N-naphthalenylimine, cyclization and oxidative removal of the N-naphthalenyl group provided a facile and ecient synthetic way to (+)-salsolidine.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract 1,4βPhenylenediamine was condensed with acetylacetone to give 4,4β²β[1,4βphenylenediβ(nitrilo)]βdipentenβ2βol **1**. Compound **1** reacted with different organic reagent to give bisazine derivatives. Β© 2004 Wiley Periodicals, Inc. Heteroatom Chem 15:293β299, 2004; Published online in Wi