Reactions of 2,4,6-Tri-t-butylphenyllithium with Deuterated Formate, Thioformate, and Selenoformate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/60/3/60_3_1037/_pdf
Reference17 articles.
1. Reactions of 2,4,6-Tri-t-butylphenyllithium withO-Alkyl Selenoformates: Intermediate Formation of 2,4,6-Tri-t-butylselenobenzaldehyde
2. Direct evidence supporting a single electron transfer pathway in the reduction of ketones by primary, secondary, and tertiary Grignard reagents
3. Reaction of Di-t-butyl Thioketone with Aryllithium. Effect of Temperature and Solvent
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1. Sequential One-Pot Addition of Excess Aryl-Grignard Reagents and Electrophiles toO-Alkyl Thioformates;Chemistry - A European Journal;2013-08-14
2. A Summary of Functional Groups Containing Selenium and Tellurium: A Catalog of the Many Groups that are Known and Some that are Not;PATAI'S Chemistry of Functional Groups;2013-06-17
3. Templated Synthesis and Intact Coordination of a Diorganotriselenane: [RuCl2(PPh3){κ3-Se,N,N‘-Se(mtSe)2}] (mtSe = selenomethimazolyl);Organometallics;2006-11-04
4. Synthesis of Se-arylmethyl selenoformates by reaction of aluminum arylmethaneselenolates with formates;Tetrahedron Letters;2005-03
5. Mesityllithium;Encyclopedia of Reagents for Organic Synthesis;2004-04-15
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