𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A High Yielding Synthesis of N-Alkyl Maleimides Using a Novel Modification of the Mitsunobu Reaction

✍ Scribed by Walker, Michael A.


Book ID
115546594
Publisher
American Chemical Society
Year
1995
Tongue
English
Weight
465 KB
Volume
60
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


The Mitsunobu reaction: A novel method f
✍ Michael A. Walker πŸ“‚ Article πŸ“… 1994 πŸ› Elsevier Science 🌐 French βš– 276 KB

Compounds l-7 were synthesized from maleimicfe and the corresponding alcohols using a novel application of the Mitsunobu reaction. This procedure allows the direct formation of a variety of bifunctional linker compounds. Bifunctional linkers, with a maleimido group attached to one end and a connecta

Synthesis of Carbocyclic Pyrimidine Nucl
✍ ElΓ­as Quezada; Dolores ViΓ±a; Giovanna Delogu; Fernanda Borges; Lourdes Santana; πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 German βš– 159 KB πŸ‘ 1 views

## Abstract The __Mitsunobu__ reaction is an important tool in carbocyclic nucleoside chemistry for the direct coupling of alcohols with heterocyclic bases under mild conditions. Chemical evidences for an unusual competitive __O__^2^‐ __vs. N__^1^‐alkylation of 3‐substituted pyrimidines is presente