𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Deprotection of benzylic esters catalysed by anhydrous ferric chloride and rhenium carbonyl compounds

✍ Scribed by Timothy J. Davies; Ray V.H. Jones; W.Edward Lindsell; Colin Miln; Peter N. Preston


Book ID
104232194
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
50 KB
Volume
43
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Anhydrous ferric chloride and [Re(CO) 4 Br] 2 are shown to be useful reagents for the catalytic deprotection of benzylic esters. A suitable protecting group is p-MeC 6 H 4 CH 2 with a working temperature of 50Β°C for debenzylation.


πŸ“œ SIMILAR VOLUMES


Carbonylation of benzyl bromide to benze
✍ Anna M Trzeciak; JΓ³zef J ZiΓ³Ε‚kowski πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 English βš– 152 KB

Ph PCH CH C O NHC CH CH SO Li in waterrtoluene solution exhibits activity in the carbonylation of benzyl 2 2 2 3 2 2 3 Ε½ . bromide to benzeneacetic acid 87% yield at 1308C and 10 atm of CO. In a reaction carried out in waterralcohol solution, corresponding esters were obtained in yields dependent o

The Synthesis of Solvent-Free Glycidic E
✍ Massimo Curini; Francesco Epifano; MariaΒ Carla Marcotullio; Ornelio Rosati πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 200 KB πŸ‘ 1 views

The results of the reaction between ethyl diazoacetate and carbonyl compounds catalysed by lanthanide triflates are described. Aldehydes, and Ξ±-unsubstituted and Ξ±-monosubstituted cyclohexanones react to give the selective formation [a