sameAs
Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts.Advances in Stereoconvergent Catalysis from 2005 to 2015: Transition-Metal-Mediated Stereoablative Reactions, Dynamic Kinetic Resolutions, and Dynamic Kinetic Asymmetric Transformations.Enantioselective Iridium-Catalyzed Allylic Alkylation Reactions of Masked Acyl Cyanide Equivalents.Potassium tert-Butoxide-Catalyzed Dehydrogenative C-H Silylation of Heteroaromatics: A Combined Experimental and Computational Mechanistic Study.Model Studies To Access the [6,7,5,5]-Core of Ineleganolide Using Tandem Translactonization-Cope or Cyclopropanation-Cope Rearrangements as Key Steps.Isocanthine Synthesis via Rh(III)-Catalyzed Intramolecular C-H Functionalization.Sequential Ruthenium Catalysis for Olefin Isomerization and Oxidation: Application to the Synthesis of Unusual Amino Acids.Ionic and Neutral Mechanisms for C-H Bond Silylation of Aromatic Heterocycles Catalyzed by Potassium tert-Butoxide.Enantioselective Total Synthesis of Nigelladine A via Late-Stage C-H Oxidation Enabled by an Engineered P450 Enzyme.Enantioselective Catalysis Coupled with Stereodivergent Cyclization Strategies Enables Rapid Syntheses of (+)-Limaspermidine and (+)-Kopsihainanine A.Catalytic Reduction of Alkyl and Aryl Bromides Using Propan-2-ol.Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates.Enantioselective Synthesis of Acyclic α-Quaternary Carboxylic Acid Derivatives through Iridium-Catalyzed Allylic Alkylation.Cyanthiwigin Natural Product Core as a Complex Molecular Scaffold for Comparative Late-Stage C-H Functionalization Studies.Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin.The Development of a Unified Enantioselective, Convergent Synthetic Approach Toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Asymmetric Formation of the Polycyclic Norditerpenoid Carbocyclic Core by Tandem Annulation CascadeOxidative Fragmentations and Skeletal Rearrangements of Oxindole Derivatives.Enantioselective Pd-Catalyzed Decarboxylative Allylic Alkylation of Thiopyranones. Access to Acyclic, Stereogenic α-Quaternary Ketones.Nickel-catalyzed enantioselective allylic alkylation of lactones and lactams with unactivated allylic alcohols.General and Practical Potassium Methoxide/Disilane-Mediated Dehalogenative Deuteration of (Hetero)ArylhalidesTotal Synthesis of the Norhasubanan Alkaloid StephadiamineCatalyst-Controlled Selective Functionalization of Unactivated C–H Bonds in the Presence of Electronically Activated C–H BondsEnantioselective synthesis of gem-disubstituted N-Boc diazaheterocycles via decarboxylative asymmetric allylic alkylation.Concise total syntheses of (–)-jorunnamycin A and (–)-jorumycin enabled by asymmetric catalysisIntramolecular Hydrogen Shift Chemistry of Hydroperoxy-Substituted Peroxy RadicalsEnantioselective Synthesis of Vicinal All-Carbon Quaternary Centers via Iridium-Catalyzed Allylic AlkylationCorrection to A Comprehensive History of Arynes in Natural Product Total SynthesisEnantioselective construction of the tricyclic core of curcusones A-D via a cross-electrophile coupling approachConcise Syntheses of Δ12-Prostaglandin J Natural Products via Stereoretentive MetathesisCatalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol CarbonatesStereospecific Overman Rearrangement of Substituted Cyclic Vinyl Bromides: Access to Fully Substituted α-Amino KetonesPalladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of 1,4-Diazepan-5-onesPalladium-Catalyzed Construction of Quaternary Stereocenters by Enantioselective Arylation of γ-Lactams with Aryl Chlorides and BromidesEnantioselective Alkynylation of Trifluoromethyl Ketones Catalyzed by Cation-Binding Salen Nickel ComplexesPalladium-Catalyzed Enantioselective Csp3-Csp3 Cross-Coupling for the Synthesis of (Poly)fluorinated Chiral Building BlocksCopper-Catalyzed Enantioselective Allylic Alkylation with a γ-Butyrolactone-Derived Silyl Ketene AcetalProgress toward the Enantioselective Synthesis of Curcusones A-D via a Divinylcyclopropane Rearrangement StrategyEnantioselective Synthesis of 15-Deoxy-Δ12,14-Prostaglandin J2Unified Enantioselective, Convergent Synthetic Approach toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Synthesis of a Series of Ineleganoloids by Oxidation-State Manipulation of the Carbocyclic CorePalladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
P50
Q38682381-45E2BA6C-E65C-478F-851D-5393A8ECB99CQ39121643-DF29633C-B397-4D80-AD0B-C35C11762D57Q41951156-62DBC7C6-2004-4052-940D-FE1F66DF559BQ44615897-69FFF7F5-BCEC-4918-BB17-501FF2F97DBAQ45972017-3180986D-D0E3-4CCB-8CEA-0F017CD61D8AQ46053546-23B2490A-07B8-4188-B267-344056FA5DBAQ46073254-916C1398-12CB-4BA1-A48E-4D3CCC0D9885Q46079170-3EBA8CBC-56CE-473A-ABFF-74615B02DAE5Q46136550-EC6531DA-CD1F-4CE9-AEFA-3A357CEEFCBEQ46203531-3729B2B1-020C-4749-8E7F-BFDB921A64A0Q46221628-F831C8BE-864E-498F-9A66-460793E04B6AQ46642667-14539A29-A45A-4BDF-B2DF-3452ACBB30BAQ47908622-422DB907-330C-46B8-BB9D-E120A89C7C6AQ48290292-1309F4C9-7333-4C21-9C9C-A3124066276DQ48315572-9588FE02-339F-49C8-8DAC-3060DDE4E968Q49717690-E6A4F816-0724-4FF2-9E05-B9785C3E1D3FQ51005109-DCEF04B8-6E92-470D-A269-784843765B03Q51814542-7D0957DC-2D22-4F46-A9C0-ECA20129A730Q55257335-CB008964-9A0B-4EEC-BB5E-25741113380EQ59723105-65B24E98-FFDC-4AA0-B224-A59EEDD4E2F7Q59752068-17FE1B3E-B1F8-4F98-B131-B12C9A5A0E84Q59944098-1EA6AD51-C476-4B38-9DF1-5F7B84F510BBQ60015130-0D23E937-3401-40DF-9DD7-B74C559C5FFAQ60363584-B3FEFD6C-97DE-4AE9-972A-926B73C0AE21Q60370200-1AAB9151-4D10-4BAE-80E6-581343F0E326Q88641144-2FA29BDC-1863-4290-9B5D-74A781216D52Q89401896-73CB6B44-F95E-4524-8E13-3DF3D1171336Q89703466-6D948773-5B6A-4B9F-8FCE-F929E59501A8Q90409196-52B0B00A-1421-4A82-A7B5-8653C79FF579Q90510939-E4BDCE40-0A86-4E46-8E3F-9DB251326DC5Q90997634-9A2AFB35-8ACA-44AA-96B5-FD464D5D4F28Q91020938-37930F16-60EC-4592-A602-5AA22EC47A0EQ91197737-81D8F352-2C4B-4AAD-907D-1687F9EB8BE3Q91241311-DE59C71E-3BD4-4CA3-BA0C-0FF98D97D466Q91295383-EF1A9BB5-9A62-4AFE-B641-94290797C022Q91337110-ACECF761-C070-45DF-B5BC-E63957CEB831Q91432901-C341CC4A-FA03-49AA-8953-C72E3D23AD08Q91751003-4F4A80DF-25B6-4B4E-BFB8-EBE4BD505986Q91843850-D3CD2949-011A-45E4-9773-13555D412C46Q92278178-2A55164E-D724-48A7-A85E-EEFFB4A71A25
P50
description
Amerikaans wetenschapper
@nl
Chemist
@en
name
Brian Stoltz
@ast
Brian Stoltz
@ca
Brian Stoltz
@en
Brian Stoltz
@es
Brian Stoltz
@fr
Brian Stoltz
@nl
type
label
Brian Stoltz
@ast
Brian Stoltz
@ca
Brian Stoltz
@en
Brian Stoltz
@es
Brian Stoltz
@fr
Brian Stoltz
@nl
altLabel
Brian M. Stoltz
@en
prefLabel
Brian Stoltz
@ast
Brian Stoltz
@ca
Brian Stoltz
@en
Brian Stoltz
@es
Brian Stoltz
@fr
Brian Stoltz
@nl
P106
P21
P2381
P31
P496
0000-0001-9837-1528
P569
1970-11-12T00:00:00Z