HIGHLY DIASTEREOSELECTIVE DIELS-ALDER REACTION MEDIATED BY A CHIRAL AUXILIARY DERIVED FROM AMINO INDANOL - THE ROLE OF CONFORMATION ON DIASTEREOSELECTIVITY

Authors
DAVIES IW SENANAYAKE CH CASTONGUAY L LARSEN RD VERHOEVEN TR REIDER PJ
Citation
Iw. Davies et al., HIGHLY DIASTEREOSELECTIVE DIELS-ALDER REACTION MEDIATED BY A CHIRAL AUXILIARY DERIVED FROM AMINO INDANOL - THE ROLE OF CONFORMATION ON DIASTEREOSELECTIVITY, Tetrahedron letters, 36(42), 1995, pp. 7619-7622
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
42
Year of publication
1995
Pages
7619 - 7622
Database
ISI
SICI code
0040-4039(1995)36:42<7619:HDDRMB>2.0.ZU;2-4
Abstract
The oxazolidinone 2 derived from amino indanol 1 functions as a very e fficient chiral auxiliary for the Diels-Alder reaction. The effect of conformation has been explored using a range of constrained phenyl gly cinol analogues.