(Q29027294)

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The boronic acid mannich reaction: A new method for the synthesis of geometrically pure allylamines

scientific article (publication date: 1993)

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The boronic acid mannich reaction: A new method for the synthesis of geometrically pure allylamines (English)

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https://doi.org/10.1016%2FS0040-4039%2800%2961625-8

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Nicos A. Petasis

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1

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https://doi.org/10.1016%2FS0040-4039%2800%2961625-8

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Irini Akritopoulou

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2

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publication date

January 1993

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https://doi.org/10.1016%2FS0040-4039%2800%2961625-8

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volume

34

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4

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583-586

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Naftifine. A review of its antimicrobial activity and therapeutic use in superficial dermatomycoses

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Synthesis and antifungal activity of (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methyl-1-naphtha lenemethanamine (SF 86-327) and related allylamine derivatives with enhanced oral activity

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Terbinafine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in superficial mycoses

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A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

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Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration

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Preparation of 3-Substituted (E)-1-Alkenylboronic Esters

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A novel route to 1,3-dienyl-2-boronic esters providing simple syntheses of conjugated [E,E]-dienes and conjugated [E]-alkenones.

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10.1016/S0040-4039(00)61625-8

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(Q29027294)

The boronic acid mannich reaction: A new method for the synthesis of geometrically pure allylamines

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