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Facial selectivity in the reactions of the cyclopentadienes 85 and 89-90

Facial selectivity in the reactions of the propellanes 36-39

Facial selectivity in the Sharnlese 6 J asymmetric dihydroxylation.

Facial selectivity of 3-indolylmethyloxaborazolidinone catalyst. Reproduced from Tetrahedron Asymmetry, 9, 357

Facial selectivity of chiral acrylates in the Diels-Alder reaction. Reproduced with permission from Oppolzer, W. Angew. Chem. Int. Ed., Engl. 1984, 23, 876. Copyright 1984 VCH Weinheim.

Facial selectivity of dihydrogen reduction controlled by phosphine ligand shape.

Facial selectivity of diphenyl pyridine-te-oxazoline catalysts. Reproduced from Tetrahedron Asymmentry, 9, 357 , by permission of Elsevier.

Facial selectivity on allylic alcohols for -dlethyl tartrate.

Facial selectivity predicted on the basis of matching of the nucleophilicity of the diene having electron-donating group X and the electrophilicity of the dienophile having electron-withdrawing group Y

Facies diagram for phyllosilicates in pelitic rocks and sediments. Zones I to VI are discussed in the text. M02 dioctahedral montmorillonites M03 trioctahedral, fully expandable phases ML

Faciie preparation of a mixed NHC PPh palladium system.

Facile 1,3-Brook reorganization of the anticipated a-keto silane adduct

Facile acylsulfonamide preparation using a sequence of immobilized reagents.

Facile and highly stereoselective and Pd catalyzed Negishi coupling .

Facile biomimetic dimerization of tetracyclic amino aldehyde 100

Facile fragmentation of Ni2CLi, 16m, in the presence of water at room temperature

Facile hydrolysis of Boc-activated amide.

Facile interconversion of frans-4-hydroxy-L-proline and c s-4-hydroxy-D-proline.

Facile microwave-assisted synthesis of a primary amide HIV-1 protease inhibitor

Facile quasi-Favorskii rearrangement.

Facile routes to skipped dienes

Facile synthesis of 2-oxo pyridinophanes 2.196 via cycloaddition of 1,6-diynes 2.195 and isocyanates.

Facile synthesis of 3,3-disubstituted 3,4-dihydroisoquinolines.

Facile synthesis of 75 from 73.

Facile synthesis of atropine .



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