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7

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年访问量

107

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总访问量

518

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1. Synthesis, biological activity, and biopharmaceutical characteriza.. [144]
2. Medium-Sized Heterocycle Synthesis by the Use of Synergistic Effec.. [140]
3. NHC-Ni catalyzed enantioselective synthesis of 1,4-dienes by cross.. [131]
4. NHC-Ni(0) Catalyzed Diastereodivergent Hydroacylative Enyne Cycliz.. [123]
5. NHC/Nickel(II)-Catalyzed [3+2] Cross-Dimerization of Unactivated O.. [112]
6. The mechanism and regioselectivities of (NHC) nickel(II) hydride-c.. [109]
7. Diastereodivergent Hydrosilylative Enyne Cyclization Catalyzed by .. [95]
8. Synthesis and study of Au(III)-indolizine derivatives: turn-on lum.. [93]
9. Computational Exploration of Mechanism and Selectivities of (NHC)N.. [92]
10. [(NHC)(NiH)-H-II]-Catalyzed Cross-Hydroalkenylation of Cyclopropen.. [84]
11. Unsymmetric N-Aryl Substituent Effects on Chiral NHC-Cu: Enantiose.. [80]
12. (NHC)NiH-Catalyzed Regiodivergent Cross-Hydroalkenylation of Vinyl.. [78]
13. Substituted 1,3-cyclohexadiene synthesis by NHC-Nickel(0) catalyze.. [72]
14. (NHC)Ni(Ⅱ)催化的[3+2]氢烯化重排串联反应的应用 [72]
15. Catalytic Asymmetric Hydroalkenylation of Vinylarenes: Electronic .. [71]
16. NHC-Ni catalyzed 1,3-and 1,4-diastereodivergent heterocycle synthe.. [70]
17. Intranasal delivery of a novel acetylcholinesterase inhibitor HLS-.. [58]
18. Transient Operation: A Catalytic Chemoselective Hydrogenation of 2.. [56]
19. Electronic Effects on Chiral NHC-Transition-Metal Catalysis [53]
20. NHC-Ni(II)-catalyzed cyclopropene-isocyanide [5+1] benzannulation [49]
21. (NHC)Pd(II) hydride-catalyzed dehydroaromatization by olefin chain.. [41]
22. Our Voyage from Catalytic Cross-Hydroalkenylation to Transfer-Dehy.. [33]
23. (NHC)Ni(II)-Directed Insertions and Higher Substituted Olefin Synt.. [22]
下载量
1. NHC-Ni catalyzed enantioselective synthesis of 1,4-dienes by cross.. [3]
2. [(NHC)(NiH)-H-II]-Catalyzed Cross-Hydroalkenylation of Cyclopropen.. [1]
3. Catalytic Asymmetric Hydroalkenylation of Vinylarenes: Electronic .. [1]
4. NHC/Nickel(II)-Catalyzed [3+2] Cross-Dimerization of Unactivated O.. [1]
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