NeoPHOX – a structurally tunable ligand system for asymmetric catalysis

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

NeoPHOX – a structurally tunable ligand system for asymmetric catalysis

A synthesis of new NeoPHOX ligands derived from serine or threonine has been developed. The central intermediate is a NeoPHOX derivative bearing a methoxycarbonyl group at the stereogenic center next to the oxazoline N atom. The addition of methylmagnesium chloride leads to a tertiary alcohol, which can be acylated or silylated to produce NeoPHOX ligands with different sterical demand. The new ...

متن کامل

MOP-phosphonites: a novel ligand class for asymmetric catalysis.

Chiral phosphonite ligands (S,R(b))-5a, (S,S(b))-5b, (R,R(b))-6a and (R,S(b))-6b are introduced, comprising a MOP-type backbone with a binol-based binaphthyl group bound to the phosphorus. Their reaction with [Pd(η(3)-C(4)H(7))Cl](2) affords η(3)-methallylpalladium chloride complexes 7a/b and 8a/b which have been isolated and structurally characterised. Solid-state and solution studies indicate...

متن کامل

Asymmetric Catalysis: Ligand Design and Conformational Studies

This thesis deals with the design of ligands for efficient asymmetric catalysis and studies of the conformation of the ligands in the catalytically active complexes. All ligands developed contain chiral oxazoline heterocycles. The conformations of hydroxyand methoxy-substituted pyridinooxazolines and bis(oxazolines) during Pd-catalysed allylic alkylations were investigated using crystallography...

متن کامل

Ligand denticity controls enantiomeric preference in DNA-based asymmetric catalysis.

DNA-based catalysis can be used to control the enantioselectivity of copper-catalysed Diels-Alder and Friedel-Crafts reactions to produce either enantiomer of the product by changing the denticity of the ligand coordinated to the Cu(II) ion, even though the DNA adopts a right handed helical conformation only.

متن کامل

Asymmetric Catalysis.

H ighlighting this issue of PNAS and the forthcoming one* is a Special Feature comprising 8 Perspectives and 44 research articles that cover aspects of asymmetric catalysis, the phenomenon whereby a chiral catalyst promotes the conversion of an achiral substrate to a chiral product with a preference for the formation of one of the mirror image isomers (enantiomers). The demand for chiral compou...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Beilstein Journal of Organic Chemistry

سال: 2016

ISSN: 1860-5397

DOI: 10.3762/bjoc.12.114