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形式
disc
反应适用性
reaction type: C-C Bond Formation
引用
SyTracks CO-Generator – J. Am. Chem. Soc. 2011, 133, 6061-6071.
Carbonylative Mizoroki-Heck – Org. Lett. 2011, 13, 2444-2447.
Primary Amides – Org. Lett. 2011, 13, 4454-4457.
Protected Acids – Org. Lett. 2012, 14, 284-287.
N-Acylation of Ureas – J. Org. Chem. 2012, 77, 3793-3799.
Carbonylative a-Arylation – Angew. Chem. Int. Ed. 2012, 51, 798-801. VIP
Protected 1,3-Ketoaldehydes – Org. Lett. 2012, 14, 2536-2539.
Alkoxy Carbonylation (ArCl) – J. Org. Chem. 2012, 77, 5357-5363.
Double Carbonylation – J. Org. Chem. 2012, 77, 6155-6165.
[14C]-Carbon Monoxide – J. Label. Compd. Radiopharm 2012, 55, 411-418.
Carbonylative Mizoroki-Heck – Org. Lett. 2011, 13, 2444-2447.
Primary Amides – Org. Lett. 2011, 13, 4454-4457.
Protected Acids – Org. Lett. 2012, 14, 284-287.
N-Acylation of Ureas – J. Org. Chem. 2012, 77, 3793-3799.
Carbonylative a-Arylation – Angew. Chem. Int. Ed. 2012, 51, 798-801. VIP
Protected 1,3-Ketoaldehydes – Org. Lett. 2012, 14, 2536-2539.
Alkoxy Carbonylation (ArCl) – J. Org. Chem. 2012, 77, 5357-5363.
Double Carbonylation – J. Org. Chem. 2012, 77, 6155-6165.
[14C]-Carbon Monoxide – J. Label. Compd. Radiopharm 2012, 55, 411-418.
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The Skrydstrup group has developed reagents and glassware for carrying out transition metal catalyzed carbonylations in a simple and safe manner.
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