Synthesis of aryl trimethylstannanes from aryl amines: A sandmeyer-type stannylation reaction
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
The invention is directed to compounds of Formula (I) described herein useful as CETP inhibitors, compositions containing them, and methods of using them.
-
Page/Page column 42-43
(2008/06/13)
Substituted fused heterocyclic herbicides
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
-
(2008/06/13)
Substituted fused heterocyclic herbicides
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
-
(2008/06/13)
Reactions of Trialkylstannane Anions R3Sn- with Arylstannanes ArSnR'3
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
Mochida, Kunio
p. 3299 - 3306
(2007/10/02)
More Articles about upstream products of 17113-81-4