Literature DB >> 17746395

Enols and other reactive species.

Y Chiang, A J Kresge.   

Abstract

Rapid advances in the chemistry of enols and other reactive species have been made possible recently by the development of methods for generating these short-lived substances in solution under conditions where they can be observed directly and their reactions can be monitored accurately. New laboratory techniques are described and a sample of the new chemistry they have made available is provided; special attention is given to ynols and ynamines and the remarkable effects that the carbon-carbon triple bonds of these substances have on their acid-base properties.

Entities:  

Year:  1991        PMID: 17746395     DOI: 10.1126/science.253.5018.395

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  6 in total

1.  Quantum chemical studies on tautomerism of barbituric acid in gas phase and in solution.

Authors:  K Senthilkumar; P Kolandaivel
Journal:  J Comput Aided Mol Des       Date:  2002-04       Impact factor: 3.686

2.  The isomerization of Δ5-androstene-3,17-dione by the human glutathione transferase A3-3 proceeds via a conjugated heteroannular diene intermediate.

Authors:  Jonathan L Daka; Ikechukwu Achilonu; Heini W Dirr
Journal:  J Biol Chem       Date:  2014-09-23       Impact factor: 5.157

3.  Prebiotic syntheses of vitamin coenzymes: II. Pantoic acid, pantothenic acid, and the composition of coenzyme A.

Authors:  S L Miller; G Schlesinger
Journal:  J Mol Evol       Date:  1993-04       Impact factor: 2.395

4.  Structure of the Escherichia coli malate synthase G:pyruvate:acetyl-coenzyme A abortive ternary complex at 1.95 A resolution.

Authors:  David M Anstrom; Karen Kallio; S James Remington
Journal:  Protein Sci       Date:  2003-09       Impact factor: 6.725

5.  Asparagine 229 in thymidylate synthase contributes to, but is not essential for, catalysis.

Authors:  L Liu; D V Santi
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-15       Impact factor: 11.205

6.  A Rh(II)-catalyzed multicomponent reaction by trapping an α-amino enol intermediate in a traditional two-component reaction pathway.

Authors:  Shunying Liu; Wenfeng Yao; Yuan Liu; Qinghua Wei; Jianghui Chen; Xiang Wu; Fei Xia; Wenhao Hu
Journal:  Sci Adv       Date:  2017-03-08       Impact factor: 14.136

  6 in total

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