๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis of protected 4-oxopipecolic acid and 4-oxolysine using a palladium-catalysed coupling process

โœ Scribed by Richard F.W. Jackson; Lisa J. Graham; Alan B. Rettie

Book ID
104214590
Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
150 KB
Volume
35
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

A synthesis of 2- and 4(5)-(2-pyridinyl)
A synthesis of 2- and 4(5)-(2-pyridinyl)imidazoles by palladium-catalysed cross-coupling reactions
โœ A.S. Bell; D.A. Roberts; K.S. Ruddock ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 198 KB

Absfrucf N-Substltuted lmldazolylzlnc chlorides were reacted wlth 2bromopyrldlne In the presence of Pd(PPh3)4 and a two-fold excess of ZnCl2 to afford cross-coupled products In 58-93% ylelds. Deprotection provlded convenient routes to 2-or 4(5)-(2-pyrtdlnyl)lmldazoles.

A versatile new synthesis of 4-aryl- and
A versatile new synthesis of 4-aryl- and heteroaryl-[3,4-c]pyrrolocarbazoles by [4+2] cycloaddition followed by palladium catalysed cross coupling
โœ Gary McCort; Olivier Duclos; Caroline Cadilhac; Eric Guilpain ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 242 KB

4-Bromo-and 4-trifluorosulfonyloxypyrrolo[3,4-c]carbazoles were prepared in five steps via a [4+2] cycloaddition and were used as key intermediates in paUadium-catalysed cross coupling reactions allowing the rapid generation of structurally diverse protein kinase C inhibitors.