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Asymmetric synthesis of samin-type lignan by Yamauchi

Asymmetric synthesis of six-membered aza-spiroindolenines by Ir-catalyzed intramolecular allylic dearomatization of indoles reported by You.

Asymmetric synthesis of sphingsine from cis- and trans-aziridines obtained by guanidinium ylide participating aziridination

Asymmetric synthesis of stegobinone starting from an

Asymmetric synthesis of streptenol A.

Asymmetric synthesis of substituted pyrrolidines by an intramolecular carbolithiation reaction .

Asymmetric synthesis of sulfonimidoyl-substituted homoallyl alcohols.

Asymmetric synthesis of syn- 2R,3S - and anfF-3-fluoroaspartic acids.

Asymmetric synthesis of tetrahydroquinoline alkaloids and drug.

Asymmetric synthesis of tetrahydroquinoline alkaloids by asymmetric transfer hydrogenation methods.

Asymmetric synthesis of tetrahydroquinoline alkaloids.

Asymmetric synthesis of tetralone 31 utilizing an enantioselective Ni-

Asymmetric synthesis of tetralone 31 utilizing an enantioselective Ni-catalyzed ring-opening of oxabenzonorbomenes.

Asymmetric synthesis of tetraphenylenes. Chiral axes for the predominant enantiomer are indicated.

Asymmetric synthesis of tetritol isomers 67 and 69. Reagents and conditions

Asymmetric synthesis of the a, a-dialkyl-a-amino acid 37 by use of -NOBIN 38.

Asymmetric synthesis of the a,a-dialkyl-a-amino acids 37 by use of the cinchona alkaloid derivative 12.

Asymmetric synthesis of the a-amino acid derivatives 26 and -27.

Asymmetric synthesis of the amino nitrile 63.

Asymmetric synthesis of the both enantiomers of a-hydroxy acids by the diastereoselective reduction of a-keto amides.

Asymmetric synthesis of the building block 95.

Asymmetric synthesis of the C-2 and C-3 stereogenic centers of nonactic acid

Asymmetric synthesis of the chiral ca-side genation. chain via catalytic hydro-

Asymmetric synthesis of the chiral co-side chain through chiral ligand-induced nucleophilic addition.

Asymmetric synthesis of the chiral co-side chain via chiral borane reduction.



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