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Nghiên cứu sử dụng vật liệu nano từ tính cofe2o4 làm chất mang xúc tác cho phản ứng knoevenagel, sonogashira, suzuki, heck

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Ngày đăng: 27/01/2021, 13:47

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Tiêu đề: Magnetically Separable Nanocatalysts: Bridges between Homogeneous and Heterogeneous Catalysis
[2] Nam T. S. Phan et al, "On the nature of the active species in palladium catalyzed Mizoroki- Heck and Suzuki-Miyaura couplings – homogeneous or heterogeneous catalysis, a critical review," Advanced Synthesis & Catalysis, vol. 348, pp. 609-679, 2006 Sách, tạp chí
Tiêu đề: On the nature of the active species in palladium catalyzed Mizoroki-Heck and Suzuki-Miyaura couplings – homogeneous or heterogeneous catalysis, a critical review
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Tiêu đề: Palladium-catalyzed cross-coupling reactions in total synthesis
[4] David H. Brown, "Evaluation of kilogram-scale Sonogashira, Suzuki, and Heck coupling routes to oncology candidate CP-724,714," Organic Process Chemical Research & Development, vol.9, pp. 440-450, 2005 Sách, tạp chí
Tiêu đề: Evaluation of kilogram-scale Sonogashira, Suzuki, and Heck coupling routes to oncology candidate CP-724,714
[5] Yoshitaka, "Acid-base catalysis of chiral Pd complexes: development of novel catalytic asymmetric reactions and their application to synthesis drug candidate," Chemical Pharmaceutical Bulletin, vol. 54, pp. 1351-1364, 2006 Sách, tạp chí
Tiêu đề: Acid-base catalysis of chiral Pd complexes: development of novel catalytic asymmetric reactions and their application to synthesis drug candidate
[6] Msashi Kishida and Hiroyuki Akita, "Synthesis of rosavin and its analogues based on a Mizoroki-Heck type reaction," Tetrahedron: Asymmetry, vol. 16, pp. 2625-2630, 2005 Sách, tạp chí
Tiêu đề: Synthesis of rosavin and its analogues based on a Mizoroki-Heck type reaction
[7] Merritt B. Andrus and Jing Liu, "Synthesis of polyhydroxylated ester analogs of the stilbene resveratrol using decarbonylative Heck couplings," Tetrahedron Letters, vol. 47, pp. 5817-5814, 2006 Sách, tạp chí
Tiêu đề: Synthesis of polyhydroxylated ester analogs of the stilbene resveratrol using decarbonylative Heck couplings
[8] Lutz F. Tietze et al, "Enantioselective palladium-catalyzed transformations," Chemical Reviews, vol. 104, pp. 3453-3516, 2004 Sách, tạp chí
Tiêu đề: Enantioselective palladium-catalyzed transformations
[9] Deniz S. DO˘GRUER et al, "Synthesis of some pyridazine derivatives carrying urea, thiourea, and sulfonamide moieties and their antimicrobial activity," Turk J Chem, vol. 34, pp. 57 – 65, 2010 Sách, tạp chí
Tiêu đề: Synthesis of some pyridazine derivatives carrying urea, thiourea, and sulfonamide moieties and their antimicrobial activity
[10] Sébastien GUÉRY et al, "A Convenient 3-Step Synthesis of 3-Acetamido-6-arylpyridazines Directed to Novel Y 5 Receptor Antagonist," Chem. Pharm. Bull., vol. 50, p. 636—639, 2002 Sách, tạp chí
Tiêu đề: A Convenient 3-Step Synthesis of 3-Acetamido-6-arylpyridazines Directed to Novel Y5 Receptor Antagonist
[11] Navnath Gavande et al, "Microwave-enhanced synthesis of 2,3,6-trisubstituted pyridazines: application to four-step synthesis of gabazine (SR-95531)," Org. Biomol. Chem., vol. 8, pp.4131–4136, 2010 Sách, tạp chí
Tiêu đề: Microwave-enhanced synthesis of 2,3,6-trisubstituted pyridazines: application to four-step synthesis of gabazine (SR-95531)
[12] Songnian Lin et al, "Total Synthesis of TMC-95A and -B via a New Reaction Leading to Z- Enamides. Some Preliminary Findings as to SAR," J. AM. CHEM. SOC., vol. 126, pp. 6347- 6355, 2004 Sách, tạp chí
Tiêu đề: Total Synthesis of TMC-95A and -B via a New Reaction Leading to Z-Enamides. Some Preliminary Findings as to SAR
[13] Dai-Shi Su et al, "Total Synthesis of (–)-Epothilone B: An Extension of the Suzuki Coupling Method and Insights into Structure–Activity Relationships of the Epothilones," Angewandte Chemie International, vol. 36, pp. 757–759, 1997 Sách, tạp chí
Tiêu đề: Total Synthesis of (–)-Epothilone B: An Extension of the Suzuki Coupling Method and Insights into Structure–Activity Relationships of the Epothilones
[14] K. C. Nicolaou et al, "Total Synthesis of Calicheamicin–Dynemicin Hybrid Molecules," Angewandte Chemie International vol. 31, pp. 340–342, 1992 Sách, tạp chí
Tiêu đề: Total Synthesis of Calicheamicin–Dynemicin Hybrid Molecules
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Tiêu đề: Total Synthesis of the Potent Microtubule-Stabilizing Agent (+)-Discodermolide
[16] Gary A. Molander and Florian Dehmel, "Formal Total Synthesis of Oximidine II via a Suzuki- Type Cross-Coupling Macrocyclization Employing Potassium Organotrifluoroborates,"ChemInform, vol. 35, 2004 Sách, tạp chí
Tiêu đề: Formal Total Synthesis of Oximidine II via a Suzuki-Type Cross-Coupling Macrocyclization Employing Potassium Organotrifluoroborates
[17] Garg NK et al, "The total synthesis of (+)-dragmacidin F," Journal of the American Chemical Society, vol. 126, pp. 9552-9553, 2004 Sách, tạp chí
Tiêu đề: The total synthesis of (+)-dragmacidin F
[18] Minoru Ikoma et al, "Synthetic studies on dragmacidin D: synthesis of the left-hand fragment," Tetrahedron Letters, vol. 49, pp. 7197–7199, 2008 Sách, tạp chí
Tiêu đề: Synthetic studies on dragmacidin D: synthesis of the left-hand fragment
[19] Neil K. Garg and Brian M. Stoltz, "The formal total synthesis of dragmacidin B, trans- dragmacidin C, and cis- and trans-dihydrohamacanthins A," Tetrahedron Letters, vol. 46, pp.2423–2426, 2005 Sách, tạp chí
Tiêu đề: The formal total synthesis of dragmacidin B, trans-dragmacidin C, and cis- and trans-dihydrohamacanthins A
[20] Toma N. Glasnov and C. Oliver Kappe, "Toward a Continuous-Flow Synthesis of Boscalid®," Advanced Synthesis & Catalysis, vol. 352, pp. 3089–3097, 2010 Sách, tạp chí
Tiêu đề: Toward a Continuous-Flow Synthesis of Boscalid®

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