Zhen‐Yu Yang scite author profile

The development of an enantioselective palladium-catalyzed 1,1-fluoroarylation of unactivated aminoalkenes is described. The reaction uses arylboronic acids as the arene source and Selectfluor as the fluorine source to generate benzylic fluorides in good yields with excellent enantioselectivities. This transformation, likely proceeding through an oxidative Heck mechanism, affords 1,1-difunctionalized alkene products.

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Unique silane modified perfluorosulfonic acids as versatile reagents for new solid acid catalysts

Harmer¹,

Sun²,

Michalczyk³

et al. 1997

Chem. Commun.

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Fluorinated organometallics: Vinyl, alkynyl, allyl, benzyl, propargyl and aryl

1994

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Genetic effect of dwarfing gene Rht13 compared with Rht-D1b on plant height and some agronomic traits in common wheat (Triticum aestivum L.)

Wang

Chen

et al. 2014

Field Crops Research

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Zhen‐Yu Yang

Fluorinated organometallics: Perfluoroalkyl and functionalized perfluoroalkyl organometallic reagents in organic synthesis

Fluorinated Ylides and Related Compounds

Effects of straw incorporation on the soil nutrient contents, enzyme activities, and crop yield in a semiarid region of China

Studies on fluoroalkylation and fluoroalkoxylation. Part 28. Palladium(0)-induced addition of fluoroalkyl iodides to alkenes: an electron transfer process

Palladium-Catalyzed Enantioselective 1,1-Fluoroarylation of Aminoalkenes

Unique silane modified perfluorosulfonic acids as versatile reagents for new solid acid catalysts

Fluorinated organometallics: Vinyl, alkynyl, allyl, benzyl, propargyl and aryl

Genetic effect of dwarfing gene Rht13 compared with Rht-D1b on plant height and some agronomic traits in common wheat (Triticum aestivum L.)

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