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Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide

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inferred← citeshttps://doi.org/10.1002/1521-3773(20000717)39:14<2536::aid-anie2536>3.0.co;2-uopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3773(20000915)39:18<3315::aid-anie3315>3.0.co;2-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3773(20011015)40:20<3842::aid-anie3842>3.0.co;2-ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3773(20020902)41:17<3192::aid-anie3192>3.0.co;2-eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470125946.ch12openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470125946.ch4openalex-snapshot
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Dimethyl sulfoxide ( DMSO )
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Dimethyl sulfoxide ( DMSO )
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Dimethyl sulfoxide ( DMSO )
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inferred← citeshttps://doi.org/10.1002/ange.200601358openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200602742openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200603653openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200604625openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200701515openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200800086openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200800626openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200802079openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200803550openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200805014openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200805334openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200805857openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201101741openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201201383openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201204992openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201205274openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201309270openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201407788openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201409629openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201501719openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201504337openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201509926openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201602125openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201711766openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201808937openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202108157openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202217809openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202405911openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202510411openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.199600171openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.199721191openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.199727411openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200300641openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200601003openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200601358openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200602742openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200603653openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200604625openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200701515openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200800086openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200800626openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200802079openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200803550openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200805014openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200805334openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200805857openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201101741openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201201383openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201204992openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201205274openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201309270openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201407788openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201409629openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201501719openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201504337openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201509926openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201602125openalex-snapshot
Concise Synthesis of a Pateamine A Analogue with In Vivo Anticancer Activity Based on an Iron‐Catalyzed Pyrone Ring Opening/Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/anie.201711766openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201808937openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202108157openalex-snapshot
Biomimetic Total Synthesis of Enterocin
inferred← citeshttps://doi.org/10.1002/anie.202217809openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202405911openalex-snapshot
Stereoconvergent Approach to the Enantioselective Construction of α‐Quaternary Alcohols by Radical Epoxide Allylation
inferred← citeshttps://doi.org/10.1002/anie.202510411openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.202001015openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bscb.19840931113openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bscb.19941030911openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cber.19741070507openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbic.200390033openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbic.201300424openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.19970031212openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200500339openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200501485openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200700057openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200700141openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200700464openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200801478openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201000795openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201000804openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201002380openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201203965openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201303915openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201400296openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201404642openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201405790openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201406256openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201503880openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201503881openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201504520openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201504674openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201600341openalex-snapshot
Total Synthesis and Complete Stereostructure of a Marine Macrolide Glycoside, (−)‐Lyngbyaloside B
inferred← citeshttps://doi.org/10.1002/chem.201605884openalex-snapshot
Harnessing a p‐Quinone Methide Intermediate in the Biomimetic Total Synthesis of the Highly Active Antibiotic 20‐Deoxy‐Elansolid B1
inferred← citeshttps://doi.org/10.1002/chem.201700476openalex-snapshot
Total Synthesis and Stereochemical Assignment of Actinoranone
inferred← citeshttps://doi.org/10.1002/chem.201704729openalex-snapshot
Quinocidin, a Cytotoxic Antibiotic with an Unusual 3,4‐Dihydroquinolizinium Ring and Michael Acceptor Reactivity toward Thiols
inferred← citeshttps://doi.org/10.1002/chem.202002404openalex-snapshot
Enantioselective Total Syntheses of (−)‐20‐epi‐Vincamine and (−)‐20‐epi‐Eburnamonine by Ir‐Catalyzed Asymmetric Imine Hydrogenation/Lactamization Cascade
inferred← citeshttps://doi.org/10.1002/chem.202200906openalex-snapshot
A Route to Lipid ALC‐0315: a Key Component of a COVID‐19 mRNA Vaccine
inferred← citeshttps://doi.org/10.1002/chem.202202464openalex-snapshot
A Vicinal Diol Approach for the Total Synthesis of Molestin E, ent ‐Sinulacembranolide A and ent ‐Sinumaximol A
inferred← citeshttps://doi.org/10.1002/chem.202301031openalex-snapshot
Converging Stereodivergent Reactions: Highly Stereoselective Formal anti‐Markovnikov Addition of H2O to Mixtures of Olefins
inferred← citeshttps://doi.org/10.1002/chem.202501531openalex-snapshot
Oxidative Dehydrogenation of N‐Heteroaromatic Alkyl Alcohols and Amines Facilitated by Dearomative Tautomerization
inferred← citeshttps://doi.org/10.1002/chir.22123openalex-snapshot
A Novel Convergent Synthesis of the Antiglaucoma PGF2α Analogue Bimatoprost
inferred← citeshttps://doi.org/10.1002/cmdc.200500057openalex-snapshot
Prins‐Type Synthesis and SAR Study of Cytotoxic Alkyl Chloro Dihydropyrans
inferred← citeshttps://doi.org/10.1002/cmdc.200900346openalex-snapshot
A Practical Total Synthesis of the Microbial Alkaline Proteinase Inhibitor (MAPI)
inferred← citeshttps://doi.org/10.1002/cmdc.200900531openalex-snapshot
A Highly Potent and Selective Caspase 1 Inhibitor that Utilizes a Key 3‐Cyanopropanoic Acid Moiety
inferred← citeshttps://doi.org/10.1002/cmdc.201300387openalex-snapshot
A Template‐Based Approach to Inhibitors of Calpain 2, 20S Proteasome, and HIV‐1 Protease
inferred← citeshttps://doi.org/10.1002/cmdc.202200486openalex-snapshot
Importance of Co‐operative Hydrogen Bonding in the Apramycin‐Ribosomal Decoding A‐Site Interaction
inferred← citeshttps://doi.org/10.1002/ejic.201402483openalex-snapshot
Triangular [Ag3]3+ Complexes Supported by Picolyl‐Substituted N‐Heterocyclic Carbene Ligands
inferred← citeshttps://doi.org/10.1002/ejoc.200700092openalex-snapshot
Chemistry of Epoxyquinols A, B, and C and Epoxytwinol A
inferred← citeshttps://doi.org/10.1002/ejoc.200700320openalex-snapshot
Solvent‐ and Structure‐Dependent Regioselectivity in the Boron‐Mediated Aldol Reaction of 2‐(1,3‐Dioxolan‐2‐yl)ethyl Ethyl Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.200800019openalex-snapshot
Nitrogen‐Containing Tricyclic and Tetracyclic Compounds by Stereoselective Samarium Diiodide Promoted Cyclizations of Quinolyl‐Substituted Ketones – A New Access to Azasteroids
inferred← citeshttps://doi.org/10.1002/ejoc.201000881openalex-snapshot
Asymmetric Synthesis of the C1–C13 Fragment of the Marine Metabolite Bistramide K
inferred← citeshttps://doi.org/10.1002/ejoc.201001104openalex-snapshot
Asymmetric Synthesis and in vivo Biological Inactivity of the Right‐Hand Terpenoid Fragment of Terpendole E
inferred← citeshttps://doi.org/10.1002/ejoc.201001268openalex-snapshot
Synthesis and Biological Evaluation of 1‐Deoxy‐5‐hydroxysphingosine Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201300083openalex-snapshot
Towards the Synthesis of Lyngbyaloside B: Stereoselective Synthesis of the C1–C16 Macrolactone Core Segment
inferred← citeshttps://doi.org/10.1002/ejoc.201300181openalex-snapshot
Synthesis of a Cn–Cn+6 Building Block Common to Important Polyol,Polyene Antibiotics from a Divinylcarbinol by a Desymmetrizing Sharpless Epoxidation
inferred← citeshttps://doi.org/10.1002/ejoc.201300257openalex-snapshot
Enantioselective Synthesis of Hushinone, Birkenol, and Birkenal
inferred← citeshttps://doi.org/10.1002/ejoc.201300643openalex-snapshot
Towards the Total Synthesis of Marineosin A: Construction of the Macrocyclic Pyrrole and an Advanced, Functionalized Spiroaminal Model
inferred← citeshttps://doi.org/10.1002/ejoc.201402234openalex-snapshot
Asymmetric Synthesis of (–)‐Pterosin N from a Chiral 1,3‐Dioxolanone
inferred← citeshttps://doi.org/10.1002/ejoc.201403140openalex-snapshot
Synthesis of Vicinal Diketoses by Using a Metathesis–Hydroxylation–Oxidation Sequence
inferred← citeshttps://doi.org/10.1002/ejoc.201500838openalex-snapshot
Asymmetric Nitrocyclopropanation of α‐Substituted α,β‐Enals Catalyzed by Diphenylprolinol Silyl Ether for the Construction of All‐Carbon Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/ejoc.201501592openalex-snapshot
Enantioselective Total Synthesis of the Proposed Structure of the Endophytic Fungal Metabolite Phomolide G: Structural Revision and Unambiguous Stereochemical Assignment
inferred← citeshttps://doi.org/10.1002/ejoc.201600142openalex-snapshot
Formal Total Synthesis of Brevisamide by Using a Tandem Isomerization/C–O and C–C Bond Formation Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201800239openalex-snapshot
Rapid Synthesis of Bicyclic N‐Heterocyclic Cores from N‐Terminal α,β‐Unsaturated Diazoketones
inferred← citeshttps://doi.org/10.1002/ejoc.201800875openalex-snapshot
Toward an Asymmetric Synthesis of Bistramide K
inferred← citeshttps://doi.org/10.1002/ejoc.201901680openalex-snapshot
A Stereoselective Formal Synthesis of Quinolizidine (–)‐217A
inferred← citeshttps://doi.org/10.1002/ejoc.202100613openalex-snapshot
Chemical Synthesis of the Nucleoside Antibiotic Capuramycin
inferred← citeshttps://doi.org/10.1002/ejoc.202300404openalex-snapshot
Synthetic Approaches to α‐, β‐, γ‐, and δ‐ L ycoranes
inferred← citeshttps://doi.org/10.1002/ejoc.202500894openalex-snapshot
Intra‐ and Intermolecular Glycosylation of d ‐Idopyranosyl and 6‐Deoxy‐ d ‐ ido ‐heptopyranosyl Donors: Toward the Repeating Unit of Campylobacter jejuni HS:4c Capsular Polysaccharide
inferred← citeshttps://doi.org/10.1002/ejoc.202501050openalex-snapshot
Total Synthesis of Bis(tetrahydroisoquinoline) Alkaloids: (−)‐Renieramycin M, (−)‐Renieramycin S, (−)‐Renieramycin T, (−)‐Jorumycin, (−)‐ Jorunnamycin A, and (−)‐Jorunnamycin C
inferred← citeshttps://doi.org/10.1002/ejoc.70589openalex-snapshot
A Comprehensive Synthetic Exploration of Euolutchuols A, B, C, and D, Hinokiol, and Related Abietane Diterpenoids
inferred← citeshttps://doi.org/10.1002/hlca.19680510818openalex-snapshot
Steroide und Sexualhormone. 236. Mitteilung [1]. Die Synthese der 5α‐ und 5β‐17‐Oxo‐19‐hydroxy‐3‐aza‐3, 19‐cyclo‐A‐homo‐androstane
inferred← citeshttps://doi.org/10.1002/hlca.19710540312openalex-snapshot
Photochemical Reactions. Part 63 [1]. The photodecarbonylation of α‐aryl aldehydes
inferred← citeshttps://doi.org/10.1002/hlca.19720550518openalex-snapshot
Steroide und Sexualhormone. 244. Mitteilung. Synthese der C‐20 epimeren 7,8‐Dihydrobatrachotoxinine
inferred← citeshttps://doi.org/10.1002/hlca.19720550823openalex-snapshot
The Photodecarbonylation of α‐Aryl Aldehydes: 1‐Formyl‐1‐methyl‐indan and heterocyclic analogues
inferred← citeshttps://doi.org/10.1002/hlca.19840670714openalex-snapshot
Experiments on the total synthesis of Lysolipin I. Part III. Preparation and transformations of substituted 1,2,3,4‐Tetrahydrodibenzofuran‐1‐ones
inferred← citeshttps://doi.org/10.1002/hlca.19930760435openalex-snapshot
A Convenient Procedure for he Synthesis o 2,3,4,6‐Tetra‐O‐benzyl‐ D ‐gluconolactam and D ‐Nojirilactam
inferred← citeshttps://doi.org/10.1002/hlca.19950780112openalex-snapshot
The Enantioselective Synthesis of the ‘Southern Part’ of Soraphen A
inferred← citeshttps://doi.org/10.1002/hlca.19980810508openalex-snapshot
Synthesis and Some Transformations of 2‐Acetamido‐5‐amino‐3,4,6‐tri‐O‐benzyl‐2,5‐dideoxy‐ D ‐glucono‐1,5‐lactam
inferred← citeshttps://doi.org/10.1002/hlca.201400291openalex-snapshot
A Stereoselective Total Synthesis of Xyolide, a Natural Bioactive Nonenolide
inferred← citeshttps://doi.org/10.1002/ijch.199100030openalex-snapshot
Asymmetric Intramolecular Ene Reaction Catalyzed by a Chiral Titanium Reagent and Synthesis of (—)‐ε‐Cadinene
inferred← citeshttps://doi.org/10.1002/ijch.201600111openalex-snapshot
Synthesis of Cryptochiral (R,R)‐2,3‐Dideuterooxirane as Stereochemical Reference Compound and Chemical Correlation with D‐(+)‐Glyceraldehyde
inferred← citeshttps://doi.org/10.1002/ijch.70001openalex-snapshot
Efficient Synthesis of p‐Tolyl 6‐Deoxy‐ d ‐Heptopyranose Thioglycosides
inferred← citeshttps://doi.org/10.1002/jhet.5570080507openalex-snapshot
Synthesis and properties of some aryl‐s‐triazines
inferred← citeshttps://doi.org/10.1002/jhet.5570120523openalex-snapshot
The photochemical synthesis of novel heterocyclic compounds from s‐triazolo[4,3‐b]pyridazine
inferred← citeshttps://doi.org/10.1002/jhet.5570290227openalex-snapshot
Synthesis of 7‐methyl‐4,6,6a,7,10,10a‐hexa‐hydroindolo[4,3‐fg]quinazoline derivatives
inferred← citeshttps://doi.org/10.1002/jlac.1991199101153openalex-snapshot
Gezielte Funktionalisierung des Pimarangerüstes, I. – Oxidationsreaktionen
inferred← citeshttps://doi.org/10.1002/jlac.199619961120openalex-snapshot
Synthetic Applications of Conjugated Nitrones, 5 A Novel Entry to the 13‐Azasteroid System
inferred← citeshttps://doi.org/10.1002/jlac.199719971107openalex-snapshot
Mukaiyama Reactions of a Silyl Enol Ether with Heteroatom‐Substituted β‐Formyl Esters
inferred← citeshttps://doi.org/10.1002/jlcr.1132openalex-snapshot
Preparation of tritium‐labeled Silybin—a protectant for common liver diseases
inferred← citeshttps://doi.org/10.1002/jlcr.2590070422openalex-snapshot
Synthesis of some radiolabeled 17α‐ethynyl‐19‐nor steroids
inferred← citeshttps://doi.org/10.1002/jps.2600740215openalex-snapshot
Synthesis of a New Anti-Inflammatory Steroidal Acid Ester: Methyl 11β-Hydroxy-3,20-Dioxo-1,4-Pregnadien-21-Oate
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