The Stille Reaction
Author:
Affiliation:
1. Boehringer Ingelheim Pharmaceuticals; Department of Process Research; Ridgefield Connecticut
2. Bayer Corp.; Department of Medicinal Chemistry; Institute for Chemistry; West Haven Connecticut
Publisher
John Wiley & Sons, Inc.
Reference890 articles.
1. ALKYLATION, ARYLATION, AND VINYLATION OF ACYL CHLORIDES BY MEANS OF ORGANOTIN COMPOUNDS IN THE PRESENCE OF CATALYTIC AMOUNTS OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(O)
2. Reaction of allyltin compounds
3. REACTIONS OF ALLYLTIN COMPOUNDS III. ALLYLATION OF AROMATIC HALIDES WITH ALLYLTRIBUTYLTIN IN THE PRESENCE OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(O)
4. A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium
5. The cross-coupling reactions of organic halides with organic derivatives of tin, mercury and copper catalyzed by palladium
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