Palladium-Catalyzed Carbonylative Cross-Coupling Reaction of Iodoalkaneswith 9-Alkyl-9-BBN Derivatives. A Direct and Selective Synthesis of Ketones

DOI: 10.1016/0040-4039(91)80445-C

Source and publish data:

Tetrahedron Letters p. 6923 - 6926 (1991)

Update date:2022-08-03

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Authors:

Ishiyama, Tatsuo

Miyaura, Norio

Suzuki, Akira

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Article abstract of DOI:10.1016/0040-4039(91)80445-C

The synthesis of unsymmetrical ketones by means of the palladium-catalyzed carbonylative cross-coupling reaction of 9-alkyl-9-BBN derivatives with iodoalkanes under a carbon monoxide atmosphere is described.

Full text of DOI:10.1016/0040-4039(91)80445-C

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Article Doi

Palladium-Catalyzed Carbonylative Cross-Coupling Reaction of Iodoalkaneswith 9-Alkyl-9-BBN Derivatives. A Direct and Selective Synthesis of Ketones

DOI: 10.1016/0040-4039(91)80445-C

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(91)80445-C

Full text of DOI:10.1016/0040-4039(91)80445-C

Products guided by the article

R&D Labs maybe for 138943-65-4

Relevant to this article

Synthesis, crystal structure, antioxidation and DNA-binding studies of a zinc(II) complex with the bis(N-allylbenzimidazol-2-ylmethyl)aniline

Heterobifunctional ligands: Practical chemoenzymatic synthesis of a cell adhesive glycopeptide that interacts with both selectins and integrins

Asymmetric dihydroxylation onto the α,β-unsaturated carboxylic ester derivatives of camptothecin

Alkenylborane-derived frustrated Lewis pairs: Metal-free catalytic hydrogenation reactions of electron-deficient alkenes

α-Amination of keto-nitrones via Multihetero-Cope rearrangement employing an imidoyl chloride reagent

Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: A facile synthetic protocol of pyrrolo[1,2-a]indoles