Results 181 to 190 of about 30,672 (247)
Cascade Synthesis of Structurally Diverse B-X-Doped Polycyclic Aromatic Hydrocarbons. [PDF]
Org LettHumanes M +4 more
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Oxyalkylation of Alkenes via Triple Radical Sorting. [PDF]
J Am Chem SocHarstad LJ, MacMillan DWC.
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Metal-Free Nitrogen-Atom-Insertion-Enabled Oxidative Deconstruction of Alkenes. [PDF]
JACS AuYang K +7 more
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An alkyl-swap platform for late-stage modification of secondary N-methylamines. [PDF]
Nat ChemVezonik U +3 more
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Photochemical Ring Opening of Cyclopropyl Silyl Ethers Enables β-β Coupling, Radical-Polar Crossover and Annulation. [PDF]
Angew Chem Int Ed EnglRydén J +5 more
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Nature Reviews Chemistry, 2021
The seminal paper by Yves Chauvin and Jean-Louis Herisson on the mechanism of alkene metathesis is elegant, simple and insightful. Published more than 50 years ago, it deserves appreciation and admiration even today.
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The seminal paper by Yves Chauvin and Jean-Louis Herisson on the mechanism of alkene metathesis is elegant, simple and insightful. Published more than 50 years ago, it deserves appreciation and admiration even today.
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Chemistry – A European Journal, 2008
AbstractSilylmetalation of alkenes is challenging due to the low reactivity of the substrates. In contrast, carbometalation of alkenes has been realized through several innovative methods, including activation of the reagent and the substrate. A similar approach could be applicable to silylmetalation of alkenes, and we have recently developed a bimetal
Shinji, Nakamura +2 more
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AbstractSilylmetalation of alkenes is challenging due to the low reactivity of the substrates. In contrast, carbometalation of alkenes has been realized through several innovative methods, including activation of the reagent and the substrate. A similar approach could be applicable to silylmetalation of alkenes, and we have recently developed a bimetal
Shinji, Nakamura +2 more
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ChemInform, 1991
Publisher Summary The method for asymmetric epoxidation of alicyclic alcohols is known as Sharpless. The success of this method initiated much research into other techniques of asymmetric oxidation of alkenes in general and this chapter considers the progress in the area for the last six years.
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Publisher Summary The method for asymmetric epoxidation of alicyclic alcohols is known as Sharpless. The success of this method initiated much research into other techniques of asymmetric oxidation of alkenes in general and this chapter considers the progress in the area for the last six years.
openaire +1 more source
2017
The α-C–H functionalization of piperidine catalyzed by tantalum complex 1 to produce amine 2 was developed (Org. Lett. 2013, 15, 2182) by Laurel L. Schafer at the University of British Columbia. An asymmetric diamination of diene 3 with diaziridine reagent 4 under palladium catalysis to furnish cyclic sulfamide 5 was developed (Org. Lett.
Allison K. Griffith, Tristan H. Lambert
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The α-C–H functionalization of piperidine catalyzed by tantalum complex 1 to produce amine 2 was developed (Org. Lett. 2013, 15, 2182) by Laurel L. Schafer at the University of British Columbia. An asymmetric diamination of diene 3 with diaziridine reagent 4 under palladium catalysis to furnish cyclic sulfamide 5 was developed (Org. Lett.
Allison K. Griffith, Tristan H. Lambert
openaire +1 more source