The Two Alternative Rate-Determining Steps in Benzylic Lithiation Reactions of Esters and Carbamates-Reference-Cited by-同舟云学术

The Two Alternative Rate-Determining Steps in Benzylic Lithiation Reactions of Esters and Carbamates

Published:2016-10-21 Issue:21 Volume:18 Page:5520-5523
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fernández-Nieto Fernando¹,Paleo M. Rita¹,Colunga Roberto¹,Raposo M. Luz²,Garcia-Rio Luis²,Sardina F. Javier¹

Affiliation:

1. Departamento de Química Orgánica and Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain

2. Departamento de Química Física and Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain

Funder

Ministerio de Economía y Competitividad

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b02753

Reference49 articles.

1. Stereo- and regiocontrol by complex induced proximity effects: reactions of organolithium compounds

2. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics

3. What’s Going on with These Lithium Reagents?

4. Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms

5. Intramolecularly chelated di- and tetranuclear aryllithium compounds: crystal structure of Li4[C6H4(2-CH2NMe2)]4 containing 4-center 2-electron-bonded C(aryl) atoms and heptacoordinate lithium atoms

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