Reaction of methyl diazoacetate with aldehydes, amines, thiols, alcohols and acids over transition metal-exchanged clays

Citation
P. Phukan et al., Reaction of methyl diazoacetate with aldehydes, amines, thiols, alcohols and acids over transition metal-exchanged clays, J CHEM S P1, (24), 1999, pp. 3685-3689
Citations number
25
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
ISSN journal
0300922X → ACNP
Issue
24
Year of publication
1999
Pages
3685 - 3689
Database
ISI
SICI code
0300-922X(1999):24<3685:ROMDWA>2.0.ZU;2-C
Abstract
Metal-exchanged clays (M=Rh and Cu) catalyze effectively the reaction of me thyl diazoacetate with various aldehydes, affording the corresponding beta- keto esters in high yields. They have also been effective in the decomposit ion of methyl diazoacetate to form metallocarbenes which, in turn, successf ully insert into X-H (X=N, O, S, CO2) bonds of a variety of amines, aldehyd es, thiols and acids, thereby producing the corresponding esters.