O-ALLYL ETHER AS A NEW PROTECTIVE GROUP FOR OXIMES AND ITS PALLADIUM-CATALYZED DEPROTECTION.

DOI: 10.1016/S0040-4039(00)96563-8

Source and publish data:

Tetrahedron Letters p. 4557 - 4560 (1987)

Update date:2022-08-22

Topics:

Authors:

Yamada, Toshiro

Goto, Kuniaki

Mitsuda, Yasuhiro

Tsuji, Jiro

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Article abstract of DOI:10.1016/S0040-4039(00)96563-8

Oximes are protected by O-allyl ether formation, and their palladium-catalyzed deallylation using triethylammonium formate as a reductant proceeds smoothly in boiling ethanol under mild conditions offering a good protective method for oximes.

Full text of DOI:10.1016/S0040-4039(00)96563-8

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