The Experts below are selected from a list of 120978 Experts worldwide ranked by ideXlab platform
Thomas R Ward - One of the best experts on this subject based on the ideXlab platform.
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Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water
Catalysis Letters, 2016Co-Authors: Anamitra Chatterjee, Thomas R WardAbstract:The palladium-catalyzed Suzuki–Miyaura cross-Coupling Reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future science and technologies. When designed properly, clean chemical technology can be developed in water as a Reaction medium. The technologies generated from such green chemistry endeavours may often be cheaper and more profitable. This review covers the literature on palladium-catalysed the Suzuki–Miyaura cross-Coupling Reaction in water. Graphical Abstract
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recent advances in the palladium catalyzed suzuki miyaura cross Coupling Reaction in water
Catalysis Letters, 2016Co-Authors: Anamitra Chatterjee, Thomas R WardAbstract:The palladium-catalyzed Suzuki–Miyaura cross-Coupling Reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future science and technologies. When designed properly, clean chemical technology can be developed in water as a Reaction medium. The technologies generated from such green chemistry endeavours may often be cheaper and more profitable. This review covers the literature on palladium-catalysed the Suzuki–Miyaura cross-Coupling Reaction in water.
Anamitra Chatterjee - One of the best experts on this subject based on the ideXlab platform.
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Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water
Catalysis Letters, 2016Co-Authors: Anamitra Chatterjee, Thomas R WardAbstract:The palladium-catalyzed Suzuki–Miyaura cross-Coupling Reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future science and technologies. When designed properly, clean chemical technology can be developed in water as a Reaction medium. The technologies generated from such green chemistry endeavours may often be cheaper and more profitable. This review covers the literature on palladium-catalysed the Suzuki–Miyaura cross-Coupling Reaction in water. Graphical Abstract
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recent advances in the palladium catalyzed suzuki miyaura cross Coupling Reaction in water
Catalysis Letters, 2016Co-Authors: Anamitra Chatterjee, Thomas R WardAbstract:The palladium-catalyzed Suzuki–Miyaura cross-Coupling Reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future science and technologies. When designed properly, clean chemical technology can be developed in water as a Reaction medium. The technologies generated from such green chemistry endeavours may often be cheaper and more profitable. This review covers the literature on palladium-catalysed the Suzuki–Miyaura cross-Coupling Reaction in water.
Shigeru Yamago - One of the best experts on this subject based on the ideXlab platform.
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photoinduced switching from living radical polymerization to a radical Coupling Reaction mediated by organotellurium compounds
Journal of the American Chemical Society, 2012Co-Authors: Yasuyuki Nakamura, Takahiro Arima, Sora Tomita, Shigeru YamagoAbstract:An efficient and simple method for the synthesis of symmetric macromolecules by photoinduced switching from radical polymerization to a radical Coupling Reaction is reported. Structurally well-defined telechelic polyisoprenes and ABA-triblock copolymers were prepared by successive organotellurium-mediated living radical polymerization (TERP) under thermal conditions, followed by a polymer-end radical Coupling Reaction under photoirradiation.
Nathan O. Siemers - One of the best experts on this subject based on the ideXlab platform.
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On the stereochemistry of the titanium-induced intramolecular pinacol Coupling Reaction
Tetrahedron Letters, 1993Co-Authors: John E. Mcmurry, Nathan O. SiemersAbstract:We have devised and tested a simple model for predicting the stereochemistry of the titanium-induced intramolecular pinacol Coupling Reaction. The model is based on molecular mechanics calculations of the dimethylsilyl acetals of the potential pinacol products. © 1993.
Jean-christophe Cintrat - One of the best experts on this subject based on the ideXlab platform.
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stille cross Coupling Reaction of an alpha stannyl enamide
Journal of Organic Chemistry, 2001Co-Authors: Stephanie Miniere, Jean-christophe CintratAbstract:The Stille cross-Coupling Reaction of an N-tosyl α-stannyl enamine is clearly exemplified for the first time with a wide range of halogeno derivatives. This gives access to functionalized α-substituted enamines in fair yields.
