about
Catalysts for CO2/epoxide ring-opening copolymerizationPowering the planet: chemical challenges in solar energy utilizationTandem synthesis of alternating polyesters from renewable resourcesSpectroscopic properties of Zn(salphenazine) complexes and their application in small molecule organic solar cells.Enantioselective cross-coupling of meso-epoxides with aryl halides.Lithium BINOL phosphate catalyzed desymmetrization of meso-epoxides with aromatic thiolsChiral epoxides via borane reduction of 2-haloketones catalyzed by spiroborate ester: application to the synthesis of optically pure 1,2-hydroxy ethers and 1,2-azido alcoholsInsight into the mechanism of aromatic hydroxylation by toluene 4-monooxygenase by use of specifically deuterated toluene and p-xylene.Asymmetric catalysis in complex target synthesisKinetic resolution of secondary alcohols using amidine-based catalysts.Chiral N-heterocyclic carbenes as stereodirecting ligands in asymmetric catalysis.Synthesis of axially chiral oxazoline-carbene ligands with an N-naphthyl framework and a study of their coordination with AuCl·SMe(2)Zirconium(IV)-Catalyzed Ring Opening of on-DNA Epoxides in Water.Catalytic hydrogen evolution from a covalently linked dicobaloximeSynthesis of enantiopure 1,2-azido and 1,2-amino alcohols via regio- and stereoselective ring-opening of enantiopure epoxides by sodium azide in hot water.A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactionsControlling the enantioselectivity of enzymes by directed evolution: practical and theoretical ramifications.Catalysts for CO2/epoxide copolymerisation.Recent advances with π-conjugated salen systems.Why nature chose Mn for the water oxidase in Photosystem II.Schiff bases: a short survey on an evergreen chemistry tool.Catalytic asymmetric desymmetrization approaches to enantioenriched cyclopentanes.Zinc complexes as fluorescent chemosensors for nucleic acids: new perspectives for a "boring" element.The Stepwise Reaction of Rhodium and Iridium Complexes of formula [MCl2(κ4C,N,N',P-L)] with Silver Cations: A Case of trans-Influence and Chiral Self-Recognition.Approaches towards molecular amplification for sensing.Mechanistic Studies of Gold and Palladium Cooperative Dual-Catalytic Cross-Coupling Systems.Aminodiols via stereocontrolled oxidation of methyleneaziridines.Differences in the Abilities to Mechanically Eliminate Activation Energies for Unimolecular and Bimolecular Reactions.Regiodivergent Catalysis: A Powerful Tool for Selective Catalysis.Oxidative Cyclization in Natural Product BiosynthesisTransition metal catalysis-a unique road map in the stereoselective synthesis of 1,3-polyols.Synthetic Strategies Employed for the Construction of Fostriecin and Related Natural Products.Recent advances in chiral imino-containing ligands for metal-catalyzed asymmetric transformations.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.A simple recipe for sophisticated cocktails: organocatalytic one-pot reactions--concept, nomenclature, and future perspectives.An Enantioselective Synthesis of the ABD Tricycle for (-)-Phomactin A Featuring Rawal's Asymmetric Diels-Alder Cycloaddition.Single-step synthesis of a new series of meso di-Mannich bases from the cyclic aminal (2S,7R,11S,16R)-1,8,10,17-tetraazapentacyclo[8.8.1.1.(8,17)0.(2,7)0(11,16)]icosane and p-substituted phenols.Selectivity, Compatibility, Downstream Functionalization, and Silver Effect in the Gold and Palladium Dual-Catalytic Synthesis of Lactones.Mechanistic Studies of Azaphilic versus Carbophilic Activation by Gold(I) in the Gold/Palladium Dual-Catalyzed Rearrangement of Alkenyl Vinyl AziridinesS-Methylidene Agents: Preparation of Chiral Non-Racemic Heterocycles.
P2860
Q26769629-67218172-7034-41C1-A814-E3C4A947F3A4Q28317749-A9A1BEA7-393D-4BA0-9CCD-E03539245066Q28740709-9EBB6B1A-AEF9-420B-A04B-2033E08729A4Q30683771-2BFC002E-D054-4F8C-924F-5C9B916EDCB3Q34464584-162DE583-FD25-4177-AFE1-DA83F4B55052Q34488544-390273C8-3B4F-4B0F-93D9-B43C28F36D38Q34663251-3AA786AC-5154-43A5-A199-6F6F26C16BEDQ34916692-3DE45D63-DD01-4C33-994D-26E11663A59AQ35691051-E34B1B2E-9E85-4F4D-B3E1-961A7B32690AQ35792784-634E41CA-D6FB-4BA2-8EB2-D5D59B8D8F5CQ35981088-4BDB8F39-A376-498B-809B-9BC491AEB60BQ36073590-1A75E235-77FE-480A-8EB8-136A7BC8BEC8Q36208818-5F20ABB3-862A-41BA-81C7-BDE6603CC95AQ36300902-4AE540FB-E2A3-4C87-886A-BEEDF79FF48FQ36523681-36C4B57E-A34E-40B4-A5BB-E6F7E83D841FQ36851982-6CC29D29-2184-4F9C-9F96-13FBEE0179F4Q37648687-9AF4BC16-B141-4723-A06D-E5BF2B015601Q37799733-E0E2EDC5-2876-4BF6-ACED-3633646FE99DQ37917610-78B7D136-D70F-4E5E-A6CA-751895EF2BD5Q38009664-EA397FA9-2B75-4FC9-9B34-7FA0AFAC4D5CQ38151010-44B95195-91A1-41BD-8851-A917AE6BB5F5Q38261817-977207CE-C42F-4D6F-9256-F327278DEE15Q38265666-4609B4E1-D2CC-4925-92F2-BBFE1184D628Q38658118-68C2B023-A025-413D-8737-7A18DA1B26FDQ38818221-C91366C3-EB3C-4D64-9D88-D3932F121EA2Q38831120-92F4D342-1DB4-4CBC-A6B0-BFD91B8D949DQ38859760-5812135B-2199-40CC-A907-5380747DCF3AQ38968147-0181D455-B0E1-4D43-8C71-114EBB4EB720Q38998506-A334188E-B647-4B84-9238-FD18C716682CQ39034361-83625E73-6FD6-4A83-8B5F-3FBE93BB6BCCQ39038143-62903D59-43A0-4DDD-94DD-73E82E4909D6Q39058997-67A7842D-B65D-40A8-B3CF-F4927BD53ED7Q39146432-3519FE27-B51D-4E18-9F6A-C1279A50D841Q39240715-AEF9A2A0-36CF-4DA5-BCFC-55BC235AD43EQ39719561-A7EEF0A5-3CE7-4848-AB26-CA981F3067DFQ39820674-C267FC6D-A409-45EA-91EE-D1B5809DF4A3Q41387113-A2A3547E-305A-4611-B353-9D9E15A1787CQ41838519-E323B045-B64E-4CCB-B440-203335280E9DQ41842084-32093234-F8F0-4CF5-9FB8-F0DADF890341Q42006869-2A2F7B8A-5468-4A31-93AE-BE3FADBB587E
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Asymmetric catalysis of epoxide ring-opening reactions.
@ast
Asymmetric catalysis of epoxide ring-opening reactions.
@en
type
label
Asymmetric catalysis of epoxide ring-opening reactions.
@ast
Asymmetric catalysis of epoxide ring-opening reactions.
@en
prefLabel
Asymmetric catalysis of epoxide ring-opening reactions.
@ast
Asymmetric catalysis of epoxide ring-opening reactions.
@en
P356
P1476
Asymmetric catalysis of epoxide ring-opening reactions.
@en
P2093
Jacobsen EN
P304
P356
10.1021/AR960061V
P407
P577
2000-06-01T00:00:00Z