Synthetic use of the primary kinetic isotope effect in hydrogen atom transfer: generation of α-aminoalkyl radicals-Reference-Cited by-同舟云学术

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Synthetic use of the primary kinetic isotope effect in hydrogen atom transfer: generation of α-aminoalkyl radicals

Published:2010 Issue:20 Volume:8 Page:4653
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wood Mark E.,Bissiriou Sabine,Lowe Christopher,Norrish Andrew M.,Sénéchal Katell,Windeatt Kim M.,Coles Simon J.,Hursthouse Michael B.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2010/OB/C0OB00205D

Reference29 articles.

1. Cephalosporin C biosynthesis; a branched pathway sensitive to a kinetic isotope effect

2. Controlling the regioselectivity of lithiation using kinetic isotope effects: Deuterium as a protecting group for carbon

3. Regioselective synthesis using the deuterium isotope effect

4. Aziridinomitosenes by Anionic Cyclization: Deuterium as a Removable Blocking Group

5. On the use of deuterium isotope effects in chemical synthesis

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2. Intramolecular 1,5-H transfer reaction of aryl iodides through visible-light photoredox catalysis: a concise method for the synthesis of natural product scaffolds;Chemical Communications;2016

3. Deuteration enhances catalyst lifetime in palladium-catalysed alcohol oxidation;Chemical Communications;2016

4. Solvent Choice and Kinetic Isotope Effects (KIEs) Dramatically Alter Regioselectivity in the DirectedorthoMetalation (DoM) of 1,5-Dichloro-2,4-dimethoxybenzene;Chemistry - A European Journal;2014-12-02

5. Synthetic use of the primary kinetic isotope effect in hydrogen atom transfer 2: generation of captodatively stabilised radicals;Organic & Biomolecular Chemistry;2013

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