𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


Diels–Alder Reactions as an Efficient Ro
✍ Mathias Glassner; James P. Blinco; Christopher Barner-Kowollik 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 321 KB

## 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

A high yielding route to substituted pip
✍ Patrick D Bailey; Peter D Smith; Frederick Pederson; William Clegg; Georgina M R 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 96 KB

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.