𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Investigations into the Regioselective C-Deuteration of Acyclic and Exocyclic Enolates.

✍ Scribed by Jason Eames; Gregory S. Coumbarides; Michael J. Suggate; Neluka Weerasooriya

Publisher
John Wiley and Sons
Year
2003
Weight
157 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Investigations into the regioselective C
Investigations into the regioselective C-deuteriation of enolates using a diisopropylammonium salt
✍ Gregory S. Coumbarides; Jason Eames; Neluka Weerasooriya 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 125 KB

## Abstract Results are reported on the regioselective __C__‐deuteriation of 2‐methyl tetralone using a series of diisopropylamine derived __D__‐sources. The results presented further aid the understanding of kinetic deuteriation of both ‘base‐containing’ and ‘base‐free’ enolates. Copyright © 2002

Investigations into the regioselective d
Investigations into the regioselective deuteriation of enolates derived from silyl enol ethers and enolacetates
✍ Gregory S. Coumbarides; Jason Eames; Neluka Weerasooriya 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 French ⚖ 127 KB

## Abstract Results are reported on the regioselective __C__‐deuteriation of a series of enolates derived from the addition of MeLi to the related enolacetate and silyl enol ether and discussed in terms of the similarity between these methods; comments are made on the possible role of the additive,

Investigations into the regioselective C
Investigations into the regioselective C-deuteriation of enolates derived from 2-methyl tetralone using piperidine-d11
✍ Gregory S. Coumbarides; Jason Eames; Michael J. Suggate 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 150 KB

## Abstract Results are reported on the regioselective __C__‐deuteriation of 2‐methyl tetralone using piperidine‐__d__~11~ as a deuterium source. The results presented further aid the understanding of kinetic deuteriation of amine–enolate complexes. Copyright © 2004 John Wiley & Sons, Ltd.

An investigation into the catalytic deut
An investigation into the catalytic deuteration and tritiation of dehydroproline9-buserelin
✍ J. Oehlke; T. Brankoff; M. Schmidt; M. Brudel; U. Kertscher; H. Berger 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 439 KB

## Abstract For optimizing the catalytic tritiation of peptides, the catalytic deuteration of buserelin and DhP^9^‐buserelin^1^ in DMA after reaction of DhP^9^‐buserelin were comparable in both solvents. The nonspecific incorporation of deuterium found after deuteration of buserelin was clearly low