Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones
about
'Click' generated 1,2,3-triazole based organosulfur/selenium ligands and their Pd(ii) and Ru(ii) complexes: their synthesis, structure and catalytic applications.Neutral chiral cyclopentadienyl Ru(ii)Cl catalysts enable enantioselective [2+2]-cycloadditions.Catalytic asymmetric alkynylation of alpha-imino ester: a versatile approach to optically active unnatural alpha-amino acid derivativesA remarkably effective copper(II)-dipyridylphosphine catalyst system for the asymmetric hydrosilylation of ketones in air.Artificial metalloenzymes based on biotin-avidin technology for the enantioselective reduction of ketones by transfer hydrogenation.Simple strategy for synthesis of optically active allylic alcohols and amines by using enantioselective organocatalysisRecent developments in the catalytic asymmetric synthesis of alpha- and beta-amino acids.Transient Ru-methyl formate intermediates generated with bifunctional transfer hydrogenation catalysts.cis-[1,4-Bis(diphenyl-phosphan-yl)butane-κ(2)P,P']dichlorido(cyclo-hexane-1,2-diamine-κ(2)N,N')ruthenium(II) dichloro-methane monosolvate.Efficient kinetic resolution of secondary alcohols using an organic solvent-tolerant esterase in non-aqueous medium.Chiral N-heterocyclic carbenes as stereodirecting ligands in asymmetric catalysis.Catalytic asymmetric synthesis of alpha- and beta-amino phosphonic acid derivatives.Enantioselective diamination with novel chiral hypervalent iodine catalysts.Synthesis and reactivity of BINEPINE-based chiral Fe(II) PNP pincer complexesNeutral tridentate PNP ligands and their hybrid analogues: versatile non-innocent scaffolds for homogeneous catalysis.Chiral biphenyl diphosphines for asymmetric catalysis: stereoelectronic design and industrial perspectives.Remarkably diastereoselective synthesis of a chiral biphenyl diphosphine ligand and its application in asymmetric hydrogenation.Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalystsLigand design for functional metal-organic frameworks.Asymmetric homogeneous hydrogenations at scale.Hydrogen atom storage upon Z-class borane ligand functions: an alternative approach to ligand cooperation.Recent advances in the total synthesis of cyclopropane-containing natural products.The N-H functional group in organometallic catalysis.Synthesis of binaphthyl based phosphine and phosphite ligands.Use of the anti-Prelog stereospecific alcohol dehydrogenase from Leifsonia and Pseudomonas for producing chiral alcohols.Frustrated Lewis pair chemistry: development and perspectives.A Decennary Journey towards the Efficient Asymmetric Hydrogenation of Highly Functionalized Ketones.Metal-Catalysed Transfer Hydrogenation of Ketones.Enzymes useful for chiral compound synthesis: structural biology, directed evolution, and protein engineering for industrial use.DFT study of isomers of the ruthenium dihydride complex RuH2(CO)2(AsMe2Ph)2.The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines.Transition metal catalysis-a unique road map in the stereoselective synthesis of 1,3-polyols.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.Total synthesis of indole-derived allocolchicine analogues exhibiting strong apoptosis-inducing activity.Frustration across the periodic table: heterolytic cleavage of dihydrogen by metal complexes.From 0 to II in One-Electron Steps: A Series of Ruthenium Complexes Supported by TropPPh2.Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C-H BondsProduction of (R)-3-quinuclidinol by E. coli biocatalysts possessing NADH-dependent 3-quinuclidinone reductase (QNR or bacC) from Microbacterium luteolum and Leifsonia alcohol dehydrogenase (LSADH)Bioinspired enantioselective synthesis of crinine-type alkaloids via iridium-catalyzed asymmetric hydrogenation of enones.From imine to amine: an unexpected left turn. Cis-β iron(ii) PNNP' precatalysts for the asymmetric transfer hydrogenation of acetophenone.
P2860
Q31110293-56D1C8E7-AD12-40FC-9BC9-0D780715F2B2Q33679825-E15E7F0E-B6E9-455D-BE62-38F3600B5F9CQ33913949-A2C3303E-0E9F-4FC4-9D67-D58B031E9C17Q33928572-E8A557F8-9A09-4693-80ED-7D69A6CC8C84Q33935114-BF8E9002-1753-4387-B02A-6862F1424203Q34375744-6B4C06FA-C57E-4BED-B673-949D5CD019BAQ35540235-8182788A-98D0-47BC-8C6B-6B2C8822E80BQ35787115-AE143172-8886-4C5B-87F9-99A2A62E5C32Q35934202-79FCABFF-C79E-44D5-9BEE-EA3F3E804B39Q35973267-C5212DAF-0994-4FB3-A3D0-F28F26DA8320Q35981088-EFAFEB2C-644E-43C2-AA9A-E92C291E4E9CQ36514806-66EF01B5-740C-4597-A33E-6CF01AD4DBE8Q36530486-75450181-CEC2-4835-9F93-E7C599B1F157Q36908260-928A4417-CCC5-423A-9311-30CDCB019C7DQ37616104-615C1F80-8CFC-48BB-B6A7-7364F21CA6D5Q37649239-AE968B92-3B4D-474B-8953-C9A0C8328863Q37649289-1D7DEAAB-9543-424E-8B68-626C314C9A0AQ37681284-A2B0C75B-673D-4914-BEEB-C258F5A1D1B3Q37932421-61B9A771-B032-4F64-B5F9-2A630ED598D5Q37982636-4221CDD4-C0E4-4205-838C-FA2E5D76F9D7Q37983744-FF071324-2D67-457A-94FD-982D355761C9Q38010631-34152C3C-570F-4DC6-81AE-327DA15C9674Q38087574-23FAEED1-46D6-455E-B8F0-4E34DC3FD8E3Q38115696-0331AE4E-5D97-4AB9-A4AE-B3F222B32DE0Q38194942-B81B5CD7-7759-44B8-92BB-8E0D315B43C2Q38479992-B767EEC8-54DC-4481-9EA9-3BC6C1D0EA38Q38559648-0879D27F-C8EF-492A-AFF0-F238F86A0701Q38826683-ED1F7059-B804-465B-83FE-693B135BDE9EQ38836633-EF792794-0302-4D7C-8FEA-1048EADF650AQ38863691-9DE93189-72E3-4E9C-98E5-61B256977A7BQ38927774-F0531C16-7F12-4F82-BFB9-9313052F725AQ39038143-6561EED9-D93B-4629-AA74-8BBC7D96CD2CQ39240715-F958AAF7-04B4-442A-B244-55E0A9D13161Q39289823-8CFFEDF4-F573-47A7-B13C-6D641E08247DQ39455495-B09842B0-76CB-4760-9E46-6192CEBFE9B7Q39456957-2C8A758D-AADF-462D-8606-B6701386F9F6Q39715561-6FBC46E5-BE7F-4B3F-9313-9DCF68F314CFQ41178042-132EB7B5-A974-468F-A12E-18099AC90878Q42279256-2E20EC64-281E-4FD4-B42E-5CD2E26C9300Q42281110-1083442C-B1FC-4472-99F5-2DEB9C03ACCA
P2860
Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@ast
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@en
type
label
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@ast
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@en
prefLabel
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@ast
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@en
P2860
P3181
P1433
P1476
Asymmetric Catalysis by Archit ...... ctive Hydrogenation of Ketones
@en
P2093
Ryoji Noyori
Takeshi Ohkuma
P2860
P3181
P356
10.1002/1521-3773(20010105)40:1<40::AID-ANIE40>3.0.CO;2-5
P577
2001-01-04T00:00:00Z