Preparation of acyclic a-methylene ketones: Palladium-catalyzed coupling of acid chlorides with organotin reagents

A.F. Renaldo; Hiroshi Ito

doi:10.1080/00397918708077327

Synthetic Communications

Paper

01 Nov 1987

Preparation of acyclic a-methylene ketones: Palladium-catalyzed coupling of acid chlorides with organotin reagents

View publication

Abstract

The reaction of organotin reagents with acid chlorides, catalyzed by palladium (0), provides a general entry to a-substituted unsaturated ketones. © 1987, Taylor & Francis Group, LLC. All rights reserved.

Conference paper

Reaction of α-trifluoromethylstyrene with anionic initiators

Hiroshi Ito, A.F. Renaldo, et al.

American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

Paper

Sensitive resist systems based on acid‐catalyzed polymer reactions

Hiroshi Ito, William P. England, et al.

Makromolekulare Chemie. Macromolecular Symposia

Paper

Thermal and Acid-Catalyzed Deesterification and Rearrangement of Poly(2-cyclopropyl-2-propyl 4-vinylbenzoate) and Their Application to Lithographic Imaging

Hiroshi Ito, William P. England, et al.

Macromolecules

Paper

Reactivities of methacrylate derivatives in radical polymerization as evaluated by mercury method

Mitsuru Ueda, Motokazu Mano, et al.

Journal of Polymer Science Part A: Polymer Chemistry

View all publications

Abstract

Related

Reaction of α-trifluoromethylstyrene with anionic initiators

Sensitive resist systems based on acid‐catalyzed polymer reactions

Thermal and Acid-Catalyzed Deesterification and Rearrangement of Poly(2-cyclopropyl-2-propyl 4-vinylbenzoate) and Their Application to Lithographic Imaging

Reactivities of methacrylate derivatives in radical polymerization as evaluated by mercury method