Highly selective one-pot synthesis of spirophosphoranes exhibiting reversed apicophilicity by oxidation of dianions generated from P-H spirophosphorane

Citation
K. Kajiyama et al., Highly selective one-pot synthesis of spirophosphoranes exhibiting reversed apicophilicity by oxidation of dianions generated from P-H spirophosphorane, ORG LETT, 3(12), 2001, pp. 1873-1875
Citations number
18
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
12
Year of publication
2001
Pages
1873 - 1875
Database
ISI
SICI code
1523-7060(20010614)3:12<1873:HSOSOS>2.0.ZU;2-N
Abstract
[GRAPHICS] Mild and highly selective one-pot procedures for obtaining phosphoranes tha t exhibit reversed (O-cis) apicophilicity are described. On the basis of th e procedures, O-cis phosphorane bearing an aryl group (R = 2,4,6-tri-i-prop ylphenyl) could be isolated for the first time; the procedure is also appli cable for alkyl derivatives. Particularly effective was the use of I-2 as a n oxidizing reagent.