about
.alpha.-Hydroxy esters as chiral auxiliaries in asymmetric cyclopropanations by rhodium(II)-stabilized vinylcarbenoidsSequential transformations to access polycyclic chemotypes: asymmetric crotylation and metal carbenoid reactions.One-pot synthesis of highly functionalized pyridines via a rhodium carbenoid induced ring expansion of isoxazoles.Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence.Catalyst-controlled formal [4 + 3] cycloaddition applied to the total synthesis of (+)-barekoxide and (-)-barekol.Combined C-H functionalization/Cope rearrangement with vinyl ethers as a surrogate for the vinylogous Mukaiyama aldol reaction.Convenient method for the functionalization of the 4- and 6-positions of the androgen skeleton.The combined C-H functionalization/Cope rearrangement: discovery and applications in organic synthesis.Computationally guided stereocontrol of the combined C-H functionalization/Cope rearrangementApplication of donor/acceptor-carbenoids to the synthesis of natural products.Highly stereoselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and chiral allylic alcohols.Reversal of the regiochemistry in the rhodium-catalyzed [4+3] cycloaddition between vinyldiazoacetates and dienesLabel-free cell cycle analysis for high-throughput imaging flow cytometry.Rhodium-catalyzed enantioselective vinylogous addition of enol ethers to vinyldiazoacetates.High Symmetry Dirhodium(II) Paddlewheel Complexes as Chiral CatalystsIntermolecular reactions of electron-rich heterocycles with copper and rhodium carbenoids.Rh2(R-TPCP)4-catalyzed enantioselective [3+2]-cycloaddition between nitrones and vinyldiazoacetates.Guiding principles for site selective and stereoselective intermolecular C-H functionalization by donor/acceptor rhodium carbenes.Reactions of metallocarbenes derived from N-sulfonyl-1,2,3-triazoles.Enantioselective synthesis of (-)-maoecrystal V by enantiodetermining C-H functionalizationCollective Approach to Advancing C-H Functionalization.Rhodium-catalyzed [3 + 2] annulation of indoles.Enantioselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and allylic alcohols.Catalytic asymmetric C-H activation of silyl enol ethers as an equivalent of an asymmetric Michael reaction.Rhodium-catalyzed conversion of furans to highly functionalized pyrroles.New strategic reactions for organic synthesis: catalytic asymmetric C-H activation alpha to nitrogen as a surrogate for the mannich reaction.Lewis acid induced tandem Diels-Alder reaction/ring expansion as an equivalent of a [4 + 3] cycloaddition.Enantioselective Gold(I)-catalyzed vinylogous [3 + 2] cycloaddition between vinyldiazoacetates and enol ethers.Catalytic asymmetric synthesis of pyrroloindolines via a rhodium(II)-catalyzed annulation of indoles.Metal carbene-promoted sequential transformations for the enantioselective synthesis of highly functionalized cycloheptadienes.Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step.Metabonomic and microbiological analysis of the dynamic effect of vancomycin-induced gut microbiota modification in the mouse.Stereoselective construction of nitrile-substituted cyclopropanes.C-H activation as a strategic reaction: enantioselective synthesis of 4-substituted indoles.Combined C-H activation/cope rearrangement as a strategic reaction in organic synthesis: total synthesis of (-)-colombiasin a and (-)-elisapterosin B.Synthesis of 2,2,2,-Trichloroethyl Aryl- and Vinyldiazoacetates by Palladium-Catalyzed Cross-Coupling.Catalytic asymmetric solid-phase cyclopropanation.Synthesis of Donor/Acceptor-Substituted Diazo Compounds in Flow and Their Application in Enantioselective Dirhodium-Catalyzed Cyclopropanation and C-H Functionalization.Concise syntheses of dictyodendrins A and F by a sequential C-H functionalization strategy.Diversity-oriented synthesis as a tool for identifying new modulators of mitosis.
P50
Q29396046-144D5C8B-60BE-47D7-89F1-0F515CAD8607Q33895415-C47BE716-FF6F-42E9-BF45-F612597DBB5DQ34067058-428ED89E-7012-4CAD-8C55-86156FD5F3F3Q34110201-E20D76E4-4F0D-48C5-8798-D18FF1A8774AQ34550801-D77F6D77-9119-4DE0-A6B6-6BFEB1AF4D48Q35858697-D12F52A0-52B5-488A-BCB1-ACDD203F6155Q35976240-38078875-8980-472D-A546-48F3AFEBC90BQ36044451-38265119-2987-4270-8526-5E256019036FQ36095738-24652345-1E8D-4488-9B6F-52B34B0F5D6EQ36095745-E6CEFA7C-A71A-42F4-8745-A049F244EBA2Q36146600-947A1D72-BAD0-4EA1-A146-2CDA2BA028F2Q36170359-07BF0E9B-BD5E-418E-ACBD-487E07CD7748Q36511094-E9076952-FC37-4EA9-9266-A45B3922C1FEQ36546581-7CC81A87-ECA8-40D4-8E00-EE9B2A124CCEQ36666396-077AA848-2EAB-4E2F-A698-221FEFDB148EQ36852287-68C2621C-1D5A-4F74-B3B9-E957D229AD29Q37634366-879404A0-0D86-43A6-ACB8-D3CDE7C62ACDQ37848105-CDC238D6-A77E-47AE-93A1-C0D2D5EB2C46Q38209815-DBF9B8E6-F38D-4F8D-BD37-863CA8992609Q38939303-62C5DB5A-70E9-4CA0-886D-1F6210B7A7B5Q41991910-811F677C-26D2-420C-B3BA-2DD19F57D9ECQ43213194-8FE714CC-AC5D-47D0-A92C-3AD5A94AC831Q43227591-07FF1F85-1710-4398-B482-B10E8E4D40B9Q43677450-DCAE53E2-53A8-4338-8D21-1D224BB3C0AFQ44312959-2CEFD61C-E02C-4774-B2BE-FA13AD2438F6Q44465146-2B7F4B94-BF31-499D-8306-476E94FB236FQ44783169-2EC3227E-EDE1-43BE-9093-CA79DC5D308DQ45171621-F251E5E1-4EAA-483E-851D-85D39501988EQ45179689-08A6EAAD-2201-42D9-A13F-6B77C260C5DBQ45247664-E117D5A4-91E0-4685-B9D0-D817408F6918Q45265914-51E6415A-2537-438C-9D5D-62E9C6BF458AQ46432616-0B73CC4D-58C2-4F55-A713-139DEF9E9DDCQ46726492-3C11D1E6-A1DC-4B79-A9A0-5153D257BCDAQ46908972-DA8A0C89-24BF-41BA-938D-196E9546FB52Q46944383-4436F82D-3BB2-40EB-8461-C0C1944FDBF1Q48347810-22E7AD7B-4982-4E95-AF57-052DE80DD1E6Q49312120-727654D9-E736-491E-91B0-11B0BD00198DQ50852807-6CC89A94-9BAF-4F35-83E3-504035FBEB50Q51020005-227F1BEF-6D4C-4D73-AADD-60E35D3D0FB4Q51757945-851E93B6-0F01-4E68-925D-26A7D6F1507B
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Huw Davies
@ast
Huw Davies
@en
Huw Davies
@es
Huw Davies
@nl
Huw Davies
@sl
type
label
Huw Davies
@ast
Huw Davies
@en
Huw Davies
@es
Huw Davies
@nl
Huw Davies
@sl
altLabel
Huw M. L. Davies
@en
prefLabel
Huw Davies
@ast
Huw Davies
@en
Huw Davies
@es
Huw Davies
@nl
Huw Davies
@sl
P1053
C-5598-2018
P106
P21
P31
P3829
P496
0000-0001-6254-9398