Selectivities in the Reactions of Alkyl-, Aryl- and Heterosubstituted Organotitanium Compounds Preliminary Communication-Reference-Cited by-同舟云学术

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Selectivities in the Reactions of Alkyl-, Aryl- and Heterosubstituted Organotitanium Compounds Preliminary Communication

Published:1981-02-04 Issue:1 Volume:64 Page:357-361
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Weidmann Beat,Widler Leo,Olivero Alan G.,Maycock Christopher D.,Seebach Dieter

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference27 articles.

1. Methyl-triisopropoxy-titanium, a highly selective nucleophilic methylating reagent. Preliminary Communication

2. Chemo- und diastereoselektive Addition von Alkyl- und Aryltitan(IV)-Verbindungen an Aldehyde und Ketone

3. Chemo- and Diastereoselective Addition of Alkyl- and Aryltitanium(IV) Compounds to Aldehydes and Ketones

4. Alkoxy-methyl-titanchloride

5. The preparation and properties of some σ-alkyl and σ-aryl derivatives of titanium

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3. Formyl MIDA Boronate: C 1 Building Block Enables Straightforward Access to α‐Functionalized Organoboron Derivatives;Angewandte Chemie International Edition;2020-08-13

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