2006The Journal of Organic ChemistryRequires access

Controlling Olefin Geometry with Pd Catalysis: Selective Formation of Z -olefins from Both E- and Z -Allylic Carbonates

Dietrich Steinhuebel, Michael Palucki, Ian W. Davies

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Abstract

The palladium-catalyzed formation of Z-olefins from allylic carbonates and a variety of protected dialkyl aminomalonates is reported. The reaction is selective for the Z-isomer, and either acetyl, Boc, or formyl protecting groups are tolerated. The Z-olefin product can be formed regardless of whether the E- or Z-allylic carbonate is used as starting material.

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The palladium-catalyzed formation of Z-olefins from allylic carbonates and a variety of protected dialkyl aminomalonates is reported. The reaction is selective for the Z-isomer, and either acetyl, Boc, or formyl protecting groups are tolerated. The Z-olefin product can be formed regardless of whether the E- or Z-allylic carbonate is used as starting material.

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Available abstract

The palladium-catalyzed formation of Z-olefins from allylic carbonates and a variety of protected dialkyl aminomalonates is reported. The reaction is selective for the Z-isomer, and either acetyl, Boc, or formyl protecting groups are tolerated. The Z-olefin product can be formed regardless of whether the E- or Z-allylic carbonate is used as starting material.

Key concepts: Allylic rearrangement, Olefin fiber, Catalysis, Palladium, Carbonate, Chemistry, Medicinal chemistry, Stereochemistry

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