๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

2-aryl acetals as acyl anion equivalents

โœ Scribed by A.I. Meyers; Arthur L. Campbell


Book ID
108384904
Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
183 KB
Volume
20
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Behavior of Dioxola
โœ R. A. AITKEN; A. W. THOMAS ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 35 KB ๐Ÿ‘ 2 views

Behavior of Dioxolanones as Chiral Acyl Anion Equivalents. -Deprotonation of 1,3-dioxolan-4-ones [cf. (I)] and following alkylation gives products (III). Their flash vacuum pyrolysis yields ketones (IV) (with concomitant loss of CO and acetone) showing (I) to be acyl anion equivalents. Conjugate ad

2-methylthioacetic acid and diethyl malo
โœ Barry M. Trost; Yoshinao Tamaru ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 184 KB

1 Acyl anions have rapidly become useful synthons. Thioacetals, 2 3 4 thioacetal monosulfoxides, protected cyanohydrins, and enol ethers have served in this role. The facile oxidative decarboxylation of carboxylic 5 acids makes them prime candidates as inexpensive and easily manipulated acyl anion e