about
Chromium- and manganese-salen promoted epoxidation of alkenes.A 3,4-trans-fused cyclic protecting group facilitates α-selective catalytic synthesis of 2-deoxyglycosides.Stereoselective Glycosylation of 2-Nitrogalactals Catalyzed by a Bifunctional Organocatalyst.On the mechanism of ylide-mediated cyclopropanations: evidence for a proton-transfer step and its effect on stereoselectivity.Practical and highly selective sulfur ylide mediated asymmetric epoxidations and aziridinations using an inexpensive, readily available chiral sulfide. Applications to the synthesis of quinine and quinidine.α-Selective Organocatalytic Synthesis of 2-DeoxygalactosidesAsymmetric alkene epoxidation with chromium oxo salen complexes. A systematic study of salen ligand substituentsSynthesis of P-stereogenic phosphorus compounds. Asymmetric oxidation of phosphines under Appel conditionsBromoethylsulfonium salt--a more effective annulation agent for the synthesis of 6- and 7-membered 1,4-heterocyclic compoundsRemote chiral induction in vinyl sulfonium salt-mediated ring expansion of hemiaminals into epoxide-fused azepinesAn efficient synthesis of imidazolinium salts using vinyl sulfonium saltsDiastereoselective synthesis of CF3-substituted, epoxide-fused heterocycles with β-(trifluoromethyl)vinylsulfonium saltsSynthesis of α-substituted vinylsulfonium salts and their application as annulation reagents in the formation of epoxide- and cyclopropane-fused heterocyclesSynthesis of 6- and 7-Membered N-Heterocycles Using α-Phenylvinylsulfonium SaltsBenzylation Reactions in DMF Lead to an Impurity Which Acts as an Organocatalyst Poison in Thiourea-Catalyzed GlycosylationsNon-photopic and photopic visual cycles differentially regulate immediate, early and late-phases of cone photoreceptor-mediated visionStereoselective organocatalyzed glycosylations - thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadingsSynthesis of glycosyl chlorides using catalytic Appel conditions
P50
Q34417418-07F90C39-53BD-428C-BF83-51DD76BEFBE0Q41125260-45A94BF2-9BC8-4670-8510-91620087F5FBQ41315277-2B7E3C0E-1906-4370-821E-30AE4A6A4DB0Q43049065-77BA08D7-2F79-447B-9A49-BC20366C1D43Q43184006-0FAA6E60-C61F-4394-9A37-0518A3E22581Q62603825-22979CAF-1966-40AD-8D2A-C57E8D76F397Q77066794-00CF0522-52AB-451A-98CC-37E96F1C23C7Q80610419-A101578D-DF83-419F-B205-424F8CC2F01DQ82915427-AA790E0C-A79A-421E-A356-B086A4406B1CQ83259765-96196661-3F26-41BD-981E-AC865F4B9970Q84139410-EB5201B3-5DDC-4922-BCAF-935391BEF0CDQ85645293-87B734BE-D121-49D2-80F2-22588D4450A3Q85773097-6BD563A5-55B6-49F2-9720-50974BC20658Q86330301-CFDB27D9-0C4C-4C1D-B0B3-F408BF4993D4Q88622574-3B532228-2131-45A9-96A6-9F4CB211DF8AQ90833112-D096F55C-5A24-43E9-80CD-515DCE116CF3Q91323735-076798DE-7644-4E9D-8FB4-0988C1C48656Q92336786-258D3CAB-14BB-4277-8419-982AA895E5A8
P50
description
researcher
@en
wetenschapper
@nl
name
E M McGarrigle
@en
E M McGarrigle
@nl
type
label
E M McGarrigle
@en
E M McGarrigle
@nl
prefLabel
E M McGarrigle
@en
E M McGarrigle
@nl
P106
P31
P496
0000-0001-8160-6431