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Stereoselective formation of Z-monofluoroalkenes by nickel-catalyzed defluorinative coupling of gem‑difluoroalkenes with lithium organoborates 被引量:1
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作者 Yisa Xiao Weichen Huang Qilong Shen 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第9期4277-4280,共4页
A method for stereoselective construction of Z-monofluoroalkenes by nickel-catalyzed defluorinative coupling of gem‑difluoroalkenes in mild conditions was described.The combination of lithium organoborate and ZnBr_(2)... A method for stereoselective construction of Z-monofluoroalkenes by nickel-catalyzed defluorinative coupling of gem‑difluoroalkenes in mild conditions was described.The combination of lithium organoborate and ZnBr_(2) generated in situ lithium aryl zincates,which facilitates the transmetalation step of the nickel-catalyzed cross coupling reaction. 展开更多
关键词 gem‑Difluoroalkenes Lithium organoborate DEFLUORINATION Nickel COUPLING
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INSERTION OF PTC-GENERATED DICHLOROCARBENE INTO C-B BO ND.A FACILE SYNTHESIS OF KETONES FROM ALKENES VIA ORGANOBORATES
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作者 De Jie ZHAO Tian Yi KE Chang Mei KE Zi Xing SHAN Chemistry Department,Wuhan University,Wuhan 430072 《Chinese Chemical Letters》 SCIE CAS CSCD 1993年第6期471-474,共4页
The insertion of dichlorocarbene generated from chloroform by Phase Transfer Catalysis(PTC)into carbon-boron bond of dialkylborate anions 3,obtained by method A and B,resulted in the formation of the inter- mediates 5... The insertion of dichlorocarbene generated from chloroform by Phase Transfer Catalysis(PTC)into carbon-boron bond of dialkylborate anions 3,obtained by method A and B,resulted in the formation of the inter- mediates 5,which were oxidized with alkaline hydrogen peroxide to give the corresponding dialkylketones in 36-77.9% yields. 展开更多
关键词 CI INSERTION OF PTC-GENERATED DICHLOROCARBENE INTO C-B BO ND.A FACILE SYNTHESIS OF KETONES FROM ALKENES VIA organoborateS PTC CHC TEBA OH BO ND VIA
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STUDIES ON THE REACTION OF DIALKYLALKENYLALKYNYLBORATE WITH ALLYL CARBONATE IN THE PRESENCE OF PALLADIUM COMPLEX
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作者 陈燕 邓敏智 时宁 《Chinese Science Bulletin》 SCIE EI CAS 1991年第7期570-573,共4页
The reactions of trialkylalkynylborate with many electrophiles, as the effective method, appear to have a broader and broader prospect in organic synthesis. In the presence of palladium complex, trialkylalkynylborate ... The reactions of trialkylalkynylborate with many electrophiles, as the effective method, appear to have a broader and broader prospect in organic synthesis. In the presence of palladium complex, trialkylalkynylborate can be allylated by allyl acetate, after protonation, giving 1, 4-alkadienes with high stereoselectivity. Similarly, the reaction between 展开更多
关键词 organoborate PALLADIUM COMPLEX ALLYL carbonate.
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