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The convenient reaction delivers the products in high yields and with high diastereo- and enantioselectivities. [ABSTRACT FROM AUTHOR]

The robust protocol displays a broad substrate scope and delivers the products in high yields and with very high diastereo- and enantioselectivities. [ABSTRACT FROM AUTHOR]

The title reagent (II) (<95% purity) is used without further purification due to its decomposition during distillation. [ABSTRACT FROM AUTHOR]

The asymmetric aldol addition reaction of aliphatic aldehydes with keto hydrates in presence of a copper-chiral BOX ligand catalyst affords the products with high enantioselectivities. [ABSTRACT FROM AUTHOR]

A series of optically active pyridyl methanols is available with the title reaction. [ABSTRACT FROM AUTHOR]

The rare-earth metal chloride can be recycled six times without notable loss of catalytic activity. [ABSTRACT FROM AUTHOR]

The novel cascade strategy for trifunctionalization of an acetylene bond proceeds via a sequence involving iodination, aryl migration, decarboxylation, and a second iodination. [ABSTRACT FROM AUTHOR]

Review: 143 refs. [ABSTRACT FROM AUTHOR]

In the Friedlaender annulation of aromatic o-aminonitriles (I) with carbonyl compounds (II) and (V) in the presence of zinc chloride, a new transformation is observed constituting a pair of divergent reaction. [ABSTRACT FROM AUTHOR]

An abstract of the article "Copper-Catalyzed Electrophilic Amination of Organoaluminum Nucleophiles with O-Benzoyl Hydroxylamines" by Shuangliu Zhou and colleagues is presented.

A series of novel 1′-substituted analogues of 4-aza-7,9-dideazaadenosine C-nucleoside are prepared and tested in antiviral assays. [ABSTRACT FROM AUTHOR]

New dinuclear rare earth metal amido complex SAC bearing methylene-linked pyrrolylamido ligands is effectively used for hydrophosphonylations of aromatic and aliphatic aldehydes (I) whereas, complex YPC gives better results for unactivated aliphatic, (hetero)aromatic ketones (IV). [ABSTRACT FROM AUTHOR]