๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Sulfobenzoic Acid Esters. III. The Correct Structures of the Aryl Esters

โœ Scribed by Loev, Bernard; Kormendy, Minerva

Book ID
127270139
Publisher
American Chemical Society
Year
1962
Tongue
English
Weight
603 KB
Volume
27
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

The electronic structure of aryl thiol e
The electronic structure of aryl thiol esters
โœ J.R. Grunwell; S.I. Hanhan ๐Ÿ“‚ Article ๐Ÿ“… 1973 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 473 KB

A combination of experimental data and the CNDO/Z-SCF-MO method are used to evaluate the importance of d-orbitals to the electronic structure of aryl thiol esters. The thioester group IS calculated to withdraw electron density through o and 2p,, -3d, bonding and donate by p,, -pm bonding. Electron d

Synthesis of aryl ฮฑ-keto esters via the
Synthesis of aryl ฮฑ-keto esters via the rearrangement of aryl cyanohydrin carbonate esters
โœ Nopporn Thasana; Vilailak Prachyawarakorn; Sopchok Tontoolarug; Somsak Ruchirawa ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 124 KB

A facile synthesis of aryl a-keto esters is reported involving the rearrangement of aryl cyanohydrin carbonate esters induced by the a-carbanion to the nitrile group generated by LDA. However, under similar conditions, an o-benzyloxycyanohydrin carbonate ester rearranged via a domino reaction leadin