17113-81-4Relevant academic research and scientific papers
Synthesis of aryl trimethylstannanes from aryl amines: A sandmeyer-type stannylation reaction
Qiu, Di,Meng, He,Jin, Liang,Wang, Shuai,Tang, Shengbo,Wang, Xi,Mo, Fanyang,Zhang, Yan,Wang, Jianbo
supporting information, p. 11581 - 11584 (2013/11/06)
Sandmeyer-type stannylation: Stille coupling is one of the most powerful coupling reactions for C-C bond formation, whereas there are only limited methods to access aryl stannane compounds. A mild stannylation process based on a Sandmeyer-type transformation using aromatic amines as the starting materials is described. DCE: 1,2-dichloroethane. Copyright
1,2,3,4-TETRAHYDRO-QUINOLINE DERIVATIVES AS CETP INHIBITORS
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Page/Page column 42-43, (2008/06/13)
The invention is directed to compounds of Formula (I) described herein useful as CETP inhibitors, compositions containing them, and methods of using them.
Substituted fused heterocyclic herbicides
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, (2008/06/13)
The invention relates to certain substituted fused compounds of Formula I STR1 which are useful as herbicides, and their agriculturally suitable compositions, as well as methods for their use as general or selective preemergent or postemergent herbicides
Substituted fused heterocyclic herbicides
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, (2008/06/13)
The invention relates to certain substituted fused compounds of Formula I STR1 which are useful as herbicides, and their agriculturally suitable compositions, as well as methods for their use as general or selective preemergent or postemergent herbicides
Reactions of Trialkylstannane Anions R3Sn- with Arylstannanes ArSnR'3
Mochida, Kunio
, p. 3299 - 3306 (2007/10/02)
The reactions of trialkylstannane anions R3Sn- with arylstannanes ArSnR'3 have been investigated; trialkylstannane anions with arylstannanes at 50 deg C gave substitution products ArSnR3 in good yields.Most of these substitution products are diverted to r
