Novel class of tertiary phosphine ligands based on a phospha-adamantane framework and use in the Suzuki cross-coupling reactions of aryl halides under mild conditions
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Adjabeng, G
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Adjabeng, G
Brenstrum, T
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Brenstrum, T
Wilson, J
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Wilson, J
Frampton, C
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Frampton, C
Robertson, A
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Robertson, A
Hillhouse, J
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Hillhouse, J
McNulty, J
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机构:Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
McNulty, J
Capretta, A
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Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, CanadaBrock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
Capretta, A
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机构:
[1] Brock Univ, Dept Chem, Inst Mol Catalysis, St Catharines, ON L2S 3A1, Canada
[2] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
[3] Cytec Canada Inc, Niagara Falls, ON L2E 6T4, Canada
A new class of sterically hindered phosphines based on a phospha-adamantane framework is described. Arylation or alkylation of the 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phospha-adamantane system allows for the preparation of tertiary phosphines suitable for use in palladium-catalyzed cross-coupling reactions. For example, use of a catalytic system incorporating Pd-2(dba)(3) and 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane is shown to promote the Suzuki cross-coupling of aryl iodides, bromides, and activated chlorides with a variety of aryl boronic acids at room temperature in a few hours with high yields.
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Univ Fed Rio Grande do Sul, Lab Mol Catalysis, Inst Quim, BR-91501970 Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Lab Mol Catalysis, Inst Quim, BR-91501970 Porto Alegre, RS, Brazil
Nobre, Sabrina M.
Monteiro, Adriano L.
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Univ Fed Rio Grande do Sul, Lab Mol Catalysis, Inst Quim, BR-91501970 Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Lab Mol Catalysis, Inst Quim, BR-91501970 Porto Alegre, RS, Brazil
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Jain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, IndiaJain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, India
Kempasiddaiah, Manjunatha
Kandathil, Vishal
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Jain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, IndiaJain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, India
Kandathil, Vishal
Dateer, Ramesh B.
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Jain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, IndiaJain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, India
Dateer, Ramesh B.
Sasidhar, B. S.
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Natl Inst Interdisciplinary Sci & Technol CSIR, Chem Sci & Technol Div, Organ Chem Sect, Thiruvananthapuram 695019, Kerala, IndiaJain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, India
Sasidhar, B. S.
Patil, Shivaputra A.
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Rosalind Franklin Univ Med & Sci, Coll Pharm, Pharmaceut Sci Dept, N Chicago, IL 60064 USAJain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, India
Patil, Shivaputra A.
Patil, Siddappa A.
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Jain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, IndiaJain Deemed Univ, Ctr Nano & Mat Sci, Jain Global Campus, Bangalore 562112, Karnataka, India