Electronic tuning in C-1-symmetric chelating diphosphane ligands supportedon stereogenic aryl-heteroaryl templates

Citation
F. Sannicolo et al., Electronic tuning in C-1-symmetric chelating diphosphane ligands supportedon stereogenic aryl-heteroaryl templates, SYNTHESIS-S, (15), 2001, pp. 2327-2336
Citations number
18
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
SYNTHESIS-STUTTGART
ISSN journal
00397881 → ACNP
Issue
15
Year of publication
2001
Pages
2327 - 2336
Database
ISI
SICI code
0039-7881(200111):15<2327:ETICCD>2.0.ZU;2-M
Abstract
The syntheses of a wide range of novel C-1-symmetric chelating diphosphanes with stereogenic axes are reported. These ligands feature identical or dif ferent phosphanyl groups supported on diverse atropisomeric templates based on the interconnection of five-membered heteroaromatic and six-membered ca rbocyclic rings, Easy synthetic accessibility, independent tunability of th e electronic and steric properties of the two phosphane donors, the low cos t and the good stereoselection ability of some of them obtained in an enant iopure state are the main advantageous features of this class of ligands.