机构:
Yale Univ, Energy Sci Inst, New Haven, CT 06520 USA
Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Energy Sci Inst, New Haven, CT 06520 USA
Brennan, Bradley J.
[1
,2
]
Gust, Devens
论文数: 0引用数: 0
h-index: 0
机构:
Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USAYale Univ, Energy Sci Inst, New Haven, CT 06520 USA
Gust, Devens
[3
]
Brudvig, Gary W.
论文数: 0引用数: 0
h-index: 0
机构:
Yale Univ, Energy Sci Inst, New Haven, CT 06520 USA
Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Energy Sci Inst, New Haven, CT 06520 USA
Brudvig, Gary W.
[1
,2
]
机构:
[1] Yale Univ, Energy Sci Inst, New Haven, CT 06520 USA
[2] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[3] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
Phenylsilatrane analogues containing reactive amino, bromo, boronic ester, and alkynyl functional groups for coupling reactions have been prepared. Pinacol boronic ester and ethynyl analogues were synthesized from 4-bromophenylsilatrane by palladium catalyzed reactions. The silatrane functional group was shown to be stable during the palladium catalysis procedures and silica-gel purification, making the molecules amenable to further synthetic manipulation. The described phenylsilatranes are useful building blocks for forming more complex organosilatrane species. (C) 2013 Elsevier Ltd. All rights reserved.