dimethoxycarbene

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2017
012320002017

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2017
2017
The reactions of dimethoxycarbene (DMC; 2), which was generated in situ by thermal decomposition of 2,5-dihydro-2,2-dimethoxy-5,5… (More)
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2017
2017
The nucleophilic dimethoxycarbene (DMC; 2) generated by thermal decomposition of 2,5dihydro-1,3,4-oxadiazole derivative 1 in… (More)
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2017
2017
Polycyclic ’cage’ ketones, such as pentacyclo[5.4.0.02,6.03,10.05,9]undecan-8-one (10), pentacyclo[5.4.0.02,6.03,10.05,9… (More)
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2007
2007
Dimethoxycarbene, in 2-fold or larger excess, reacts with dimethyl 2,3-dicyanomaleate and fumarate to afford an unstable… (More)
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2006
2006
The zwitterion formed by the reaction of dimethoxycarbene and DMAD adds efficiently to one of the carbonyl groups of 1,2… (More)
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2006
2006
[reaction: see text] Highly substituted beta-lactams have been isolated as the major product of the reaction of dimethoxycarbene… (More)
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2005
2005
[reaction: see text] At 50 degrees C, dimethyl dicyanofumarate and maleate react with 2 equiv of dimethoxycarbene to generate the… (More)
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2003
2003
This Account focuses mainly on our recent endeavors in the area of multicomponent reactions (MCRs) involving zwitterionic species… (More)
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2002
2002
Reaction of dimethoxycarbene (DMC), generated by thermolysis of a 2,5-dihydro-1,3,4-oxadiazole, with 2,2,4,4-tetramethyl-3… (More)
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2000
2000
The potential-energy surfaces for the abstraction reactions of carbenes with oxirane and thiirane have been characterized in… (More)
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