The Experts below are selected from a list of 106863 Experts worldwide ranked by ideXlab platform
Yang Ren - One of the best experts on this subject based on the ideXlab platform.
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sodium borohydride nickel chloride hexahydrate in etoh peg 400 as an efficient and recyclable Catalytic System for the reduction of alkenes
RSC Advances, 2018Co-Authors: Chuanchao Liu, Kang Wang, Yang RenAbstract:An efficient, safe and one-pot convenient Catalytic System has been developed for the reduction of alkenes using NaBH4–NiCl2·6H2O in EtOH/PEG-400 under mild conditions. In this Catalytic System, a variety of alkenes (including trisubstituted alkene α-pinene) were well reduced and the Ni catalyst could be recycled.
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Sodium borohydride-nickel chloride hexahydrate in EtOH/PEG-400 as an efficient and recyclable Catalytic System for the reduction of alkenes
RSC Advances, 2018Co-Authors: Chuanchao Liu, Kang Wang, Yang RenAbstract:An efficient, safe and one-pot convenient Catalytic System has been developed for the reduction of alkenes using NaBH4–NiCl2·6H2O in EtOH/PEG-400 under mild conditions. In this Catalytic System, a variety of alkenes (including trisubstituted alkene α-pinene) were well reduced and the Ni catalyst could be recycled.
Yoshihiko Yamamoto - One of the best experts on this subject based on the ideXlab platform.
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Intramolecular Hydroalkoxylation of Unactivated Alkenes Using Silane—Iodine Catalytic System.
ChemInform, 2015Co-Authors: Shoji Fujita, Masanori Abe, Masatoshi Shibuya, Yoshihiko YamamotoAbstract:The novel Catalytic System is used successfully for the preparation of a broad spectrum of substituted furans and some pyran structures.
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Intramolecular Hydroalkoxylation of Unactivated Alkenes Using Silane-Iodine Catalytic System.
Organic letters, 2015Co-Authors: Shoji Fujita, Masanori Abe, Masatoshi Shibuya, Yoshihiko YamamotoAbstract:A novel Catalytic System using I2 and PhSiH3 for the intramolecular hydroalkoxylation of unactivated alkenes is described. NMR study indicated that in situ generated PhSiH2I is a possible active Catalytic species. This Catalytic System allows an efficient intramolecular hydroalkoxylation of phenyl-, trialkyl-, and 1,1-dialkyl-substituted alkenes as well as a variety of unactivated monoalkyl- and 1,2-dialkyl-substituted alkenes at room temperature. Mechanistic consideration based on significant experimental observations is also discussed.
Chuanchao Liu - One of the best experts on this subject based on the ideXlab platform.
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sodium borohydride nickel chloride hexahydrate in etoh peg 400 as an efficient and recyclable Catalytic System for the reduction of alkenes
RSC Advances, 2018Co-Authors: Chuanchao Liu, Kang Wang, Yang RenAbstract:An efficient, safe and one-pot convenient Catalytic System has been developed for the reduction of alkenes using NaBH4–NiCl2·6H2O in EtOH/PEG-400 under mild conditions. In this Catalytic System, a variety of alkenes (including trisubstituted alkene α-pinene) were well reduced and the Ni catalyst could be recycled.
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Sodium borohydride-nickel chloride hexahydrate in EtOH/PEG-400 as an efficient and recyclable Catalytic System for the reduction of alkenes
RSC Advances, 2018Co-Authors: Chuanchao Liu, Kang Wang, Yang RenAbstract:An efficient, safe and one-pot convenient Catalytic System has been developed for the reduction of alkenes using NaBH4–NiCl2·6H2O in EtOH/PEG-400 under mild conditions. In this Catalytic System, a variety of alkenes (including trisubstituted alkene α-pinene) were well reduced and the Ni catalyst could be recycled.
Shoji Fujita - One of the best experts on this subject based on the ideXlab platform.
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Intramolecular Hydroalkoxylation of Unactivated Alkenes Using Silane—Iodine Catalytic System.
ChemInform, 2015Co-Authors: Shoji Fujita, Masanori Abe, Masatoshi Shibuya, Yoshihiko YamamotoAbstract:The novel Catalytic System is used successfully for the preparation of a broad spectrum of substituted furans and some pyran structures.
-
Intramolecular Hydroalkoxylation of Unactivated Alkenes Using Silane-Iodine Catalytic System.
Organic letters, 2015Co-Authors: Shoji Fujita, Masanori Abe, Masatoshi Shibuya, Yoshihiko YamamotoAbstract:A novel Catalytic System using I2 and PhSiH3 for the intramolecular hydroalkoxylation of unactivated alkenes is described. NMR study indicated that in situ generated PhSiH2I is a possible active Catalytic species. This Catalytic System allows an efficient intramolecular hydroalkoxylation of phenyl-, trialkyl-, and 1,1-dialkyl-substituted alkenes as well as a variety of unactivated monoalkyl- and 1,2-dialkyl-substituted alkenes at room temperature. Mechanistic consideration based on significant experimental observations is also discussed.
Kang Wang - One of the best experts on this subject based on the ideXlab platform.
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sodium borohydride nickel chloride hexahydrate in etoh peg 400 as an efficient and recyclable Catalytic System for the reduction of alkenes
RSC Advances, 2018Co-Authors: Chuanchao Liu, Kang Wang, Yang RenAbstract:An efficient, safe and one-pot convenient Catalytic System has been developed for the reduction of alkenes using NaBH4–NiCl2·6H2O in EtOH/PEG-400 under mild conditions. In this Catalytic System, a variety of alkenes (including trisubstituted alkene α-pinene) were well reduced and the Ni catalyst could be recycled.
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Sodium borohydride-nickel chloride hexahydrate in EtOH/PEG-400 as an efficient and recyclable Catalytic System for the reduction of alkenes
RSC Advances, 2018Co-Authors: Chuanchao Liu, Kang Wang, Yang RenAbstract:An efficient, safe and one-pot convenient Catalytic System has been developed for the reduction of alkenes using NaBH4–NiCl2·6H2O in EtOH/PEG-400 under mild conditions. In this Catalytic System, a variety of alkenes (including trisubstituted alkene α-pinene) were well reduced and the Ni catalyst could be recycled.
