๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

ChemInform Abstract: Primary Amides. A General Nitrogen Source for Catalytic Asymmetric Aminohydroxylation of Olefins.

โœ Scribed by Zachary P. Demko; Michael Bartsch; K. Barry Sharpless

Publisher
John Wiley and Sons
Year
2000
Weight
31 KB
Volume
31
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

ChemInform Abstract: N-Chloro-N-sodio-2-
ChemInform Abstract: N-Chloro-N-sodio-2-trimethylsilyl Ethyl Carbamate: A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation.
โœ K. L. REDDY; K. R. DRESS; K. B. SHARPLESS ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 33 KB ๐Ÿ‘ 1 views

Asymmetric aminohydroxylation of the alkenes (I) and (IV) is performed with the title carbamate using an asymmetric catalyst. The silyl protecting group of the products is readily cleaved with fluoride under mild conditions. -

ChemInform Abstract: Heterogeneous Catal
ChemInform Abstract: Heterogeneous Catalytic Asymmetric Aminohydroxylation of Olefins Using Polymer-Supported Cinchona Alkaloids.
โœ E. Nandanan; Prodeep Phukan; Godwin C. G. Pais; A. Sudalai ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 1 views

Heterogeneous Catalytic Asymmetric Aminohydroxylation of Olefins Using Polymer-Supported Cinchona Alkaloids. -The first heterogeneous asymmetric aminohydroxylation catalyzed by OsO 4 using polymer supported cinchona alkaloid is reported. However, the reactions only proceed with moderate enantiosele