Efficient synthesis of six-membered ring D analogues of the pentacyclic alkaloid cephalotaxine by two palladium-catalyzed reactions

Citation
Lf. Tietze et al., Efficient synthesis of six-membered ring D analogues of the pentacyclic alkaloid cephalotaxine by two palladium-catalyzed reactions, EUR J ORG C, (13), 2000, pp. 2433-2444
Citations number
44
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
1434193X → ACNP
Issue
13
Year of publication
2000
Pages
2433 - 2444
Database
ISI
SICI code
1434-193X(200007):13<2433:ESOSRD>2.0.ZU;2-O
Abstract
D-homo-Cephalotaxine analogues 19 and 23 have been prepared by intramolecul ar Heck reactions of 12 and 22. The substrates 12 and 22 were obtained by a lkylation and acylation, respectively, of the spirocyclic amines 17, which in turn, were generated by intramolecular palladium-catalyzed allylic amina tion.