The reaction of carbamoylcopper with a silyl chloride to give a carbamoylsilane
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference19 articles.
1. Acyllithium to lithium enolate conversion by a 1,2-silicon shift. A shortcut to acylsilane enolates
2. Intramolecular conversions of acyllithium. Cyclization in the reaction of carbon monoxide with [1-(silyl)vinyl]lithium
3. Strategy for the Use of Acyllithium in Synthesis: Intramolecular Conversion;Murai,1992
4. A Reagent for Direct Nucleophilic Carbamoylation
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1. Acylsilanes: valuable organosilicon reagents in organic synthesis;Chemical Society Reviews;2013
2. Synthesis and Properties of Secondary Thiocarbamoylsilanes;Bulletin of the Chemical Society of Japan;2010-01-15
3. Acyl Silanes;PATAI'S Chemistry of Functional Groups;2009-12-15
4. A Facile Synthesis of Carbamoylsilanes, ‐boranes and ‐phosphane Oxides – Isolation of the First Uncomplexed Carbamoylborane;European Journal of Inorganic Chemistry;2006-12
5. Functions Containing a Carbonyl Group and Two Heteroatoms Other Than a Halogen or Chalcogen;Comprehensive Organic Functional Group Transformations II;2005
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