𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reductive formylation of N,N-dimethyl-p-nitrosoaniline by glyoxylic acid. Evidence for a hydroxamic acid intermediate

✍ Scribed by Corbett, Michael D.; Corbett, Bernadette R.

Book ID
121364452
Publisher
American Chemical Society
Year
1981
Tongue
English
Weight
443 KB
Volume
46
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Reactions of peroxynitrite with N,N-dime
Reactions of peroxynitrite with N,N-dimethyl-p-toluidine and 1,4-naphthoquinone. Evidence for heterolytic cleavage of a nitrogenξ—Έoxygen bond in peroxynitrous acid
✍ Nobuaki Nonoyama; Kaori Hisatome; Chizuru Shoda; Hitomi Suzuki πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 129 KB

Peroxynitrite (ONOO-) has been found to react with the title amine 1 and quinone 5 to form N-nitrosoamine 2 and 2,3-epoxide 6, respectively, in accord with the in situ generation of the nitrosonium and hydroperoxide ions as the respective reactive species.

An efficient synthesis of a key intermed
An efficient synthesis of a key intermediate for the preparation of the rhinovirus protease inhibitor AG7088 via asymmetric dianionic cyanomethylation of N-Boc-l-(+)-glutamic acid dimethyl ester
✍ Qingping Tian; Naresh K Nayyar; Srinivasan Babu; Lijian Chen; Junhua Tao; Steven πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 65 KB

An efficient synthetic route to a key intermediate for the preparation of the rhinovirus protease inhibitor AG7088 has been developed employing a key asymmetric dianionic cyanomethylation of N-Boc-L-(+)-glutamic acid dimethyl ester. This methodology enables the preparation of this compound in kilogr