Study of the Lithiated Phenylacetonitrile Monoanions and Dianions Formed According to the Lithiated Base Used (LHMDS, LDA, or n-BuLi). 2. Alkylation and Deuteriation Mechanism Study by Vibrational and NMR Spectroscopy and Quantum Chemistry Calculations-Reference-Cited by-同舟云学术

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Study of the Lithiated Phenylacetonitrile Monoanions and Dianions Formed According to the Lithiated Base Used (LHMDS, LDA, or n-BuLi). 2. Alkylation and Deuteriation Mechanism Study by Vibrational and NMR Spectroscopy and Quantum Chemistry Calculations

Published:2012-07-23 Issue:15 Volume:77 Page:6431-6442
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Strzalko Tekla¹,Wartski Lya¹,Corset Jacques²,Castellà-Ventura Martine³,Froment Françoise²

Affiliation:

1. LSOM - CNRS/U-PSUD, Institut de Chimie Moléculaire et des Matériaux d’Orsay, 15 Rue Georges Clémenceau, 91405 Orsay Cedex, France

2. LADIR - CNRS/UPMC, 4 Place Jussieu, 75252 Paris Cedex 05, France

3. LCT - CNRS/UPMC, 4 Place Jussieu, 75252 Paris Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo300758g

Reference59 articles.

1. Study of the Lithiated Phenylacetonitrile Monoanions and Dianions Formed According to the Lithiated Base Used (LHMDS, LDA, or n-BuLi). 1. Evidence of Heterodimer (“Quadac”) or Dianion Formation by Vibrational Spectroscopy

2. gem-Dialkali derivatives of certain functionally substituted organic compounds

3. Synthesis and Reactivity of sp3-Geminated Organodimetallics

4. Stereoselective Synthesis of 2-Alkylidene-3-iminoindoles by Reaction of 1,1-Dianions with Oxalic Acid Bis(imidoyl) Chlorides

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