Strongly Preferential Alkylation and Carbonyl Olefination of α- and β-Hydroxycarbonyl Compounds by Organo-Transition Metal Reagents in Competition Experiments with the Corresponding Deoxy Compounds-Reference-Cited by-同舟云学术

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Strongly Preferential Alkylation and Carbonyl Olefination of α- and β-Hydroxycarbonyl Compounds by Organo-Transition Metal Reagents in Competition Experiments with the Corresponding Deoxy Compounds

Published:1985-04 Issue:4 Volume:24 Page:348-350
ISSN:0570-0833
Container-title:Angewandte Chemie International Edition in English
language:en
Short-container-title:Angew. Chem. Int. Ed. Engl.

Author:

Kauffmann Thomas,Möller Thomas,Rennefeld Heidi,Welke Siegfried,Wieschollek Raphael

Publisher

Wiley

Reference13 articles.

1. Überraschende Stabilität nucleophiler CrIII-Alkylierungs- und -Allylierungsreagentien gegen Ethanol und Wasser

2. Aldehydspezifische und aldehydselektive alkylierungen mit organoniob- und - tantal-reagenzien (1)

3. Chelat- oder Nicht-Chelat-Kontrolle bei Additionsreaktionen von chiralen α- und β-Alkoxycarbonyl-Verbindungen

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1. Additions of Organomagnesium Halides to α-Alkoxy Ketones: Revision of the Chelation-Control Model;Organic Letters;2017-06-15

2. A Unified Approach to the Daucane and Sphenolobane Bicyclo[5.3.0]decane Core: Enantioselective Total Syntheses of Daucene, Daucenal, Epoxydaucenal B, and 14-para-Anisoyloxydauc-4,8-diene;Chemistry - A European Journal;2013-12-02

3. Organotitanium Chemistry;Organometallics in Synthesis: A Manual;2013-06-26

4. Titanium in Organic Synthesis;Organometallics in Synthesis;2013-06-26

5. Reagents for Carbonyl Methylenation in Organic Synthesis;Current Organic Synthesis;2005-04-01

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