"DEUTERATED" RANEY NICKEL: DEUTERATION (REDUCTION) OF ALKENES, CARBONYL COMPOUNDS AND AROMATIC RINGS. PROTON-DEUTERIUM EXCHANGE OF "ACTIVATED" ALIPHATIC AND AROMATIC RING HYDROGENS.

DOI: 10.1016/S0040-4039(01)81217-X

Source and publish data:

Tetrahedron Letters p. 2507 - 2508 (1984)

Update date:2022-08-05

Topics:: Authors:

Pojer, Peter M.

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Article abstract of DOI:10.1016/S0040-4039(01)81217-X

In the absence of deuterium gas, the reaction of deuterated Raney nickel with benzene derivatives, carbonyl compounds, alkenes and activated methylene grops gave either fully deuterated (reduced) products or led to hydrogen-deuterium exchange.

Full text of DOI:10.1016/S0040-4039(01)81217-X

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Article Doi

"DEUTERATED" RANEY NICKEL: DEUTERATION (REDUCTION) OF ALKENES, CARBONYL COMPOUNDS AND AROMATIC RINGS. PROTON-DEUTERIUM EXCHANGE OF "ACTIVATED" ALIPHATIC AND AROMATIC RING HYDROGENS.

DOI: 10.1016/S0040-4039(01)81217-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(01)81217-X

Full text of DOI:10.1016/S0040-4039(01)81217-X

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