Metal-free organocatalysis through explicit hydrogen bonding interactions.
about
Bronsted acid catalysis of achiral enamine for regio- and enantioselective nitroso aldol synthesisThe Halogen BondApplications of helical-chiral pyridines as organocatalysts in asymmetric synthesis.Influence of the substitution and conformation of C--H-bond-based bis-triazole acceptors in anion-binding catalysis.Structural optimization of thiourea-based bifunctional organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones.Non-bonding 1,5-S···O interactions govern chemo- and enantioselectivity in isothiourea-catalyzed annulations of benzazoles.Enantioselective thiourea-catalyzed additions to oxocarbenium ions.Quantum mechanical investigations of organocatalysis: mechanisms, reactivities, and selectivities.Chemoenzymatic synthesis of each enantiomer of orthogonally protected 4,4-difluoroglutamic acid: a candidate monomer for chiral Brønsted acid peptide-based catalystsChiral N-Heterocyclic Carbene Catalyzed Annulations of Enals and Ynals with Stable Enols: A Highly Enantioselective Coates-Claisen Rearrangement.A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactionsKinetic evidence of an apparent negative activation enthalpy in an organocatalytic process.Crystal structures of N-[(4-phenyl-thia-zol-2-yl)carbamo-thio-yl]benzamide and N-{[4-(4-bromo-phen-yl)thia-zol-2-yl]carbamo-thio-yl}benzamide from synchrotron X-ray diffraction.Exploring the potential of diarylacetylenediols as hydrogen bonding catalysts.To protonate or alkylate? Stereoselective Brønsted acid catalysis of C-C bond formation using diazoalkanes.Oxazolones in organocatalysis, new tricks for an old reagent.Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitriles.Recent advances in enantioselective organocatalyzed anhydride desymmetrization and its application to the synthesis of valuable enantiopure compounds.Developing novel organocatalyzed aldol reactions for the enantioselective synthesis of biologically active molecules.Low-loading asymmetric organocatalysis.Transfer hydrogenation with Hantzsch esters and related organic hydride donors.Asymmetric organocatalytic addition reactions of maleimides: a promising approach towards the synthesis of chiral succinimide derivatives.Applications of asymmetric organocatalysis in medicinal chemistry.Bifunctional primary amine-thioureas in asymmetric organocatalysis.Beyond click chemistry - supramolecular interactions of 1,2,3-triazoles.N,N'-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea: a privileged motif for catalyst development.Asymmetric catalysis mediated by the ligand sphere of octahedral chiral-at-metal complexes.Catalytic oxidation of biorefinery lignin to value-added chemicals to support sustainable biofuel production.Thiourea-catalyzed enantioselective cyanosilylation of ketones.London dispersion in molecular chemistry--reconsidering steric effects.Active sites on graphene-based materials as metal-free catalysts.Metal-organic and covalent organic frameworks as single-site catalysts.Cooperative Trifunctional Organocatalysts for Proficient Proton Transfer Reactions.Metal organic frameworks mimicking natural enzymes: a structural and functional analogy.New approaches to organocatalysis based on C-H and C-X bonding for electrophilic substrate activationDetoxifying polyhalogenated catechols through a copper-chelating agent by forming stable and redox-inactive hydrogen-bonded complexes with an unusual perpendicular structure.Exploiting Octahedral Stereocenters: From Enzyme Inhibition to Asymmetric Photoredox Catalysis.Organocatalytic Transfer Hydrogenation and Hydrosilylation Reactions.Asymmetric Brønsted acid catalysis with chiral carboxylic acids.Rapid quantification of the activating effects of hydrogen-bonding catalysts with a colorimetric sensor.
P2860
Q24548097-637C3E5F-63DD-4E4C-87B8-0BC566787666Q28077775-3BA90B8E-88B1-47D6-9BC8-D46F58BC20A4Q30578194-C4C06D62-8880-479B-9606-9DC9A4B2FA73Q30833949-5D1AEBB1-81A3-4D95-801A-16DF72C53063Q33263511-34938E47-2576-4D2F-83BE-580075C44AB5Q33744327-A610C8DC-9B6C-40B0-A7B8-A4925371A64DQ34778549-F986A1DA-448D-40B9-BF18-08DE21C86FB6Q35159601-16D9850A-C63E-44F7-9B12-15E0C9025A0EQ35586035-009D4B0C-A201-40A8-AA91-3B3E60645C12Q35857313-56B4C293-078F-4B32-A880-E57014B79D1CQ36851982-E7E204DA-D190-4812-92BD-7F52D474B569Q37132563-6790F565-BA93-49B2-935C-2BF23E1A0D2EQ37432507-20332FD8-92B5-43C5-9D43-BE38CAA0E03DQ37670416-C0BBD739-AF00-40D7-9728-2A3A6F8A8DBFQ37704260-432EDF9F-0F39-4CD4-B424-301C11FAAC08Q37846197-F5FBD5DF-0534-453C-B9FE-A2D7A16281B5Q37870065-8B4BD04B-7CB1-43E2-A5BF-949989B633D6Q37898012-C92B00EB-71E2-40FE-8DA2-401FFA7C950FQ37932392-5CC6B30C-0690-4431-BA0F-B595AAD54D53Q37968170-274D9425-ED02-465E-A1C6-9E9AA93BA7D3Q37979197-1504F422-FAF7-4FC1-880A-90D5E961A1C2Q38045277-9BAD3E89-A2F7-4BD3-A159-2BFE35CD9097Q38060074-84DAEA02-E76D-4396-9762-F1A888089311Q38140730-2F887CF7-0314-410C-A6AF-D842E4E94A6AQ38184880-C58C728E-E4B4-41B3-B7A9-DD5E3355588CQ38202902-EFD9CF05-45AA-40CB-B6E9-E7885AE1885CQ38243303-0AF884D5-DAC9-45B0-99B0-B6CCC164F8A4Q38255891-8B67801C-9A4D-4ADB-A45E-302828FFD9B2Q38304709-24EAA023-CA15-4844-9D40-0B69C3F747F2Q38564398-EDAF9B9F-42D6-489E-A644-1339298590F0Q38676255-FF82B9D8-7D0B-4C95-A1FE-7E5206F945A8Q38740514-26CF70EA-9A24-49C7-8886-8C6E33034139Q38806641-4A229B99-B632-4D9C-836C-F63393195B85Q38850656-892642AE-C896-47E6-8045-4A2BA92DB1CCQ39112697-122331F2-F677-454B-B05A-CF754AC04927Q39144652-EBF14640-656A-41A1-B0EB-FDB797016E3DQ39192964-D62D08FB-613D-4213-A940-D263A6AEB12FQ39442487-1D70AE93-12F3-463E-BBDF-C00538A46D97Q39449464-0E83DD9A-520A-42F1-B347-7DAADFB53FD7Q41470187-6F61EACE-59E9-4055-8962-63A6EE90CB5B
P2860
Metal-free organocatalysis through explicit hydrogen bonding interactions.
description
2003 nî lūn-bûn
@nan
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@ast
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@en
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@nl
type
label
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@ast
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@en
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@nl
prefLabel
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@ast
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@en
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@nl
P356
P1476
Metal-free organocatalysis through explicit hydrogen bonding interactions.
@en
P2093
Peter R Schreiner
P304
P356
10.1039/B107298F
P577
2003-09-01T00:00:00Z