Reactions of [Aryloxy(phenyl)carbene]pentacarbonylchromium(0) Complexes with Thiolate Ions. Decreasing Reactivity with Increasing Basicity of the Nucleophile-Reference-Cited by-同舟云学术

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Reactions of [Aryloxy(phenyl)carbene]pentacarbonylchromium(0) Complexes with Thiolate Ions. Decreasing Reactivity with Increasing Basicity of the Nucleophile

Published:2007-11-15 Issue:25 Volume:72 Page:9456-9463
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bernasconi Claude F.¹,Pérez-Lorenzo Moisés¹,Codding Sara J.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Santa Cruz, California 95064

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo701422z

Reference46 articles.

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Effects of substituents on activation parameter changes in the Michael-type reactions of nucleophilic addition to activated alkenes and alkynes in solution;Monatshefte für Chemie - Chemical Monthly;2015-12-16

2. Activation Parameter Changes as a Mechanistic Tool in Acyl-Transfer Reactions in Solution;Current Organic Chemistry;2014-06-25

3. Fischer carbene complexes remain favourite targets, and vehicles for new discoveries;Dalton Trans.;2014

4. Towards mechanisms of bimolecular nucleophilic reactions in solution-probing the variation of the activation parameters in the reactions of aromatic compounds;Journal of Physical Organic Chemistry;2011-08-02

5. Substituent effects on the activation parameters of SNar reactions;Russian Journal of Organic Chemistry;2010-01

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