science
plus
.abes.fr
|
explorer
À propos de :
Doyle Michael P.
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
foaf:Person
, within Data Space :
scienceplus.abes.fr
associated with source
document(s)
Type:
Person
New Facet based on Instances of this Class
Attributs
Valeurs
type
Person
name
Doyle Michael P.
familyName
Doyle
Given name
Michael P.
is
relates
of
http://hub.abes.fr/acs/periodical/joceah/1976/volume_41/issue_8/101021jo00870a022/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1984/volume_49/issue_11/101021jo00185a014/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1989/volume_54/issue_16/101021jo00277a009/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1975/volume_40/issue_26/101021jo00914a003/authorship/1
http://hub.abes.fr/acs/periodical/orgnd7/1984/volume_3/issue_1/101021om00079a010/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_19/101021ja00072a021/authorship/5
http://hub.abes.fr/acs/periodical/chreay/1986/volume_86/issue_5/101021cr00075a013/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1977/volume_42/issue_11/101021jo00431a021/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1995/volume_60/issue_10/101021jo00115a018/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1978/volume_43/issue_4/101021jo00398a039/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1981/volume_46/issue_25/101021jo00338a008/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_25/101021jo061411m/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_13/101021jo050609o/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_16/101021jo049403y/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_17/101021ja061146m/authorship/4
http://hub.abes.fr/acs/periodical/orgnd7/2002/volume_21/issue_9/101021om011082i/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_21/101021jo0614902/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_12/101021ja070122s/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_42/101021ja045330o/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_50/101021ja066452e/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2000/volume_122/issue_24/101021ja9945414/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_23/101021jo00049a010/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1975/volume_40/issue_26/101021jo00914a004/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_8/101021jo00384a049/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1973/volume_38/issue_15/101021jo00955a022/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_26/101021jo00261a045/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1992/volume_114/issue_5/101021ja00031a048/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1990/volume_112/issue_5/101021ja00161a040/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1992/volume_114/issue_7/101021ja00033a081/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_10/101021jo00210a020/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1982/volume_47/issue_21/101021jo00142a013/authorship/1
http://hub.abes.fr/acs/periodical/achre4/1986/volume_19/issue_11/101021ar00131a004/authorship/1
http://hub.abes.fr/acs/periodical/orgnd7/1984/volume_3/issue_1/101021om00079a011/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1975/volume_40/issue_26/101021jo00914a002/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1972/volume_94/issue_10/101021ja00765a084/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1987/volume_109/issue_5/101021ja00239a038/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_22/101021ja00075a013/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1974/volume_39/issue_18/101021jo00932a015/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1984/volume_49/issue_7/101021jo00181a010/authorship/1
http://hub.abes.fr/acs/periodical/orgnd7/1994/volume_13/issue_4/101021om00016a012/authorship/1
is
Author
of
Dirhodium(II) tetrakis(carboxamidates) with chiral ligands. Structure and selectivity in catalytic metal-carbene transformations
Catalytic methods for metal carbene transformations
Correlations between catalytic reactions of diazo compounds and stoichiometric reactions of transition-metal carbenes with alkenes. Mechanism of the cyclopropanation reaction
Silane reductions in acidic media. 9. The effect of Lewis acids on stereoselectivities in ketone reductions. The principle of complexation-induced conformational perturbation. Energy minimization in the transition states for hydride transfer
Catalytic role of copper triflate in Lewis acid promoted reactions of diazo compounds
Silane reductions in acidic media. V. Reductions of alkyl-substituted cyclohexanones by di- and tri-tert-butylsilanes. Steric hindrance to nucleophilic attack at silicon in the trifluoroacetolysis of silyl alkyl ethers
Outer-sphere one-electron reductions of arenediazonium salts
Silane reductions in acidic media. VI. Mechanism of organosilane reductions of carbonyl compounds. Transition state geometries of hydride transfer reactions
Synthesis and catalytic reactions of chiral N-(diazoacetyl)oxazolidones
Formation and characterization of 3-O-arenediazoascorbic acids. New stable diazo ethers
Spirolactones from Dirhodium(II)-Catalyzed Diazo Decomposition with Regioselective Carbon-Hydrogen Insertion
Stereoselectivity of catalytic cyclopropanation reactions. Catalyst dependence in reactions of ethyl diazoacetate with alkenes
Silane reductions in acidic media. I. Reduction of aldehydes and ketones in alcoholic acidic media. General synthesis of ethers
Silane reductions in acidic media. VII. Aluminum chloride catalyzed hydrogen-halogen exchange between organosilanes and alkyl halides. An efficient hydrocarbon synthesis
High enantioselectivity for intermolecular cyclopropenation of alkynes by diazo esters catalyzed by chiral dirhodium(II) carboxamides
Silane reductions in acidic media. II. Reductions of aryl aldehydes and ketones by trialkylsilanes in trifluoroacetic acid. Selective method for converting the carbonyl group to methylene
Silane reductions in acidic media. IV. Reductions of alkyl-substituted cyclohexanones by mono-, di-, and trialkylsilanes. Stereochemistry of alcohol and ether formation
Rearrangements of ylides generated from reactions of diazo compounds with allyl acetals and thioketals by catalytic methods. Heteroatom acceleration of the [2,3]-sigmatropic rearrangement
Ligand effects on dirhodium(II) carbene reactivities. Highly effective switching between competitive carbenoid transformations
Perspective on Dirhodium Carboxamidates as Catalysts
Enantiocontrolled Macrocycle Formation by Catalytic IntramolecularCyclopropanation
The Oxidative Mannich Reaction Catalyzed by Dirhodium Caprolactamate
Vinyldiazolactone as a Vinylcarbene Precursor: Highly Selective C−HInsertion and Cyclopropanation Reactions
Polyether Macrocycles from Intramolecular Cyclopropanationand Ylide Formation. Effect of Catalyst and Coordination
“Matched/Mismatched” Diastereomeric Dirhodium(II)Carboxamidate Catalyst Pairs. Structure−Selectivity Correlationsin Diazo Decomposition and Hetero-Diels−Alder Reactions
Divergence of Carbonyl Ylide Reactions as a Function ofDiazocarbonyl Compound and Aldehyde Substituent: Dioxolanes,Dioxolenes, and Epoxides
Bis(phenyl)dirhodium(III) Caprolactamate: A Dinuclear Paddlewheel Complexwith No Metal−Metal Bond
Preparation and Catalytic Properties of ImmobilizedChiral Dirhodium(II) Carboxamidates
Dirhodium(II) Caprolactamate: An Exceptional Catalyst for Allylic Oxidation
Exceptionally high trans (anti) stereoselectivity in catalytic cyclopropanation reactions
A new and general synthesis of .alpha.-silyl carbonyl compounds by silicon-hydrogen insertion from transition metal-catalyzed reactions of diazo esters and diazo ketones
Electrophilic metal carbenes as reaction intermediates in catalytic reactions
Control of chemoselectivity in catalytic carbenoid reactions. Dirhodium(II) ligand effects on relative reactivities
Highly Regioselective and Stereoselective Silylformylation of Alkynes Under Mild Conditions Promoted by Dirhodium(II) Perfluorobutyrate
Enantioselective metal carbene transformations with polyethylene-bound soluble recoverable dirhodium(II) 2-pyrrolidone-5(S)-carboxylates
Silane reductions in acidic media. 10. Ionic hydrogenation of cycloalkenes. Stereoselectivity and mechanism
Highly effective catalytic methods for ylide generation from diazo compounds. Mechanism of the rhodium- and copper-catalyzed reactions with allylic compounds
Cyclopropanation of .alpha.,.beta.-unsaturated carbonyl compounds and nitriles with diazo compounds. The nature of the involvement of transition-metal promoters
Silane reductions in acidic media. III. Reductions of aldehydes and ketones to alcohols and alcohol derivatives. General syntheses of alcohols, symmetrical ethers, carboxylate esters and acetamides
Unsymmetrical alkenes by carbene coupling from diazirine decomposition in the presence of diazo compounds
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
