Synthesis of [13C6]3,4-diaminobenzoic acid as a precursor for stable isotope labeled benzimidazoles-Reference-Cited by-同舟云学术

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Synthesis of [13C6]3,4-diaminobenzoic acid as a precursor for stable isotope labeled benzimidazoles

Published:2017-04 Issue:17 Volume:58 Page:1692-1694
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Donahue Matthew G.,Jentsch Nicholas G.,Simons Casey R.

Funder

University of Southern Mississippi

National Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Isotopic Labeling of Metabolites in Drug Discovery Applications

2. Application of Stable Isotope-Labeled Compounds in Metabolism and in Metabolism-Mediated Toxicity Studies

3. The use of stable isotope labelling for the analytical chemistry of drugs

4. Impact of kinetic isotope effects in isotopic studies of metabolic systems

5. 13C Metabolic Flux Analysis

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1. Imidazoles;Comprehensive Heterocyclic Chemistry IV;2022

2. Heteroleptic thiolate diamine nickel complexes: Noble-free-metal catalysts in electrocatalytic and light-driven hydrogen evolution reaction;International Journal of Hydrogen Energy;2021-05

3. Transition-metal-free mono- or dinitration of protected anilines;Synthetic Communications;2020-04-21

4. Five-Membered Ring Systems;Progress in Heterocyclic Chemistry;2018

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