An efficient route to aminoanthraquinones and derivatives via a diels-alder reaction.
✍ Scribed by Mohamed Chigr; Houda Fillion; Annie Rougny
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 218 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
CycloaddLGoti od 1 EJ -I-N-catLbobenzoxyatnLno-J ,3-buX.adiene Xo naptiuqtinunen ~ok%xued by a..tomo.aZztion a6 the adduots and dep4oZetion 06 Xhe amino ghoup addotid heghon&~tive hyathtbeb OQ -5 and -b ubntitied arnLnoantktaqu.inoneb.
📜 SIMILAR VOLUMES
## Abstract A simple and efficient route for the synthesis of cyclic polymer systems is presented. Linear furan protected __α__‐maleimide‐__ω__‐cyclopentadienyl functionalized precursors (poly(methyl methacrylate) and poly(__tert__‐butyl acrylate)) were synthesized via atom transfer radical polymer
The imine Ph 2 CHN CHCO 2 Et, generated from benzhydrylamine and ethyl glyoxylate, is an excellent dienophile in aza-Diels-Alder reactions, giving diastereomerically pure cycloadducts in high yield.