REACTIVITY OF DIFFERENTIALLY SUBSTITUTED BIS(DIAZO) ESTERS IN RHODIUM(II) MEDIATED O-H INSERTION REACTIONS

Citation
Cj. Moody et Dj. Miller, REACTIVITY OF DIFFERENTIALLY SUBSTITUTED BIS(DIAZO) ESTERS IN RHODIUM(II) MEDIATED O-H INSERTION REACTIONS, Tetrahedron, 54(10), 1998, pp. 2257-2268
Citations number
49
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
54
Issue
10
Year of publication
1998
Pages
2257 - 2268
Database
ISI
SICI code
0040-4020(1998)54:10<2257:RODSBE>2.0.ZU;2-E
Abstract
Selective catalysed decompositions of one diazo group in the presence of another are discussed. A range of bis(diazo) compounds was prepared in which the two diazo groups are differentially substituted. Rhodium (II) acetate catalysed decomposition in the presence of methanol resul ted in exclusive O-H insertion reaction at the more reactive diazo gro up, the less reactive diazophosphonate remaining intact. With the more active rhodium(II) trifluoroacetamide as catalyst, both diazo groups decomposed simultaneously. (C) 1998 Elsevier Science Ltd. All rights r eserved.