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Catalytic Asymmetric Dihydroxylation
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inferred← citeshttps://doi.org/10.2139/ssrn.4160521openalex-extracted
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inferred← citeshttps://doi.org/10.2139/ssrn.4658963openalex-extracted
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inferred← citeshttps://doi.org/10.1002/(sici)1097-461x(2000)77:2<544::aid-qua6>3.0.co;2-lopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0682(199903)1999:3<471::aid-ejic471>3.0.co;2-hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199801)1998:1<149::aid-ejoc149>3.0.co;2-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199801)1998:1<21::aid-ejoc21>3.0.co;2-0openalex-snapshot
Polymer-Supported Catalytic Asymmetric Sharpless Dihydroxylations of Olefins
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199806)1998:6<1155::aid-ejoc1155>3.0.co;2-gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199808)1998:8<1569::aid-ejoc1569>3.0.co;2-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199809)1998:9<1923::aid-ejoc1923>3.0.co;2-bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199811)1998:11<2673::aid-ejoc2673>3.0.co;2-copenalex-snapshot
A Novel Concept for Transition-Metal-Catalyzed Reactions: Electron Transfer under Buffered Protic Conditions
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199905)1999:5<1075::aid-ejoc1075>3.0.co;2-iopenalex-snapshot
Enantioselective Synthesis of the Chromane Moiety of Vitamin E
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199905)1999:5<959::aid-ejoc959>3.0.co;2-kopenalex-snapshot
Synthesis Mediated by Ring-Closing Metathesis – Applications in the Synthesis of Azasugars and Alkaloids
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199909)1999:9<2167::aid-ejoc2167>3.0.co;2-lopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199911)1999:11<2965::aid-ejoc2965>3.0.co;2-hopenalex-snapshot
Synthesis of (–)-Cytoxazone, a Novel Cytokine Modulator Isolated fromStreptomyces sp.
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(200001)2000:2<349::aid-ejoc349>3.0.co;2-jopenalex-snapshot
A Facile Route to Bulladecin-Type Acetogenins - Total Synthesis of Asimilobinand Correction of the Configuration of Its Tetrahydrofuran Segment
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(200002)2000:3<401::aid-ejoc401>3.0.co;2-mopenalex-snapshot
Studies on the Mercury-Desilylation of Chiral Cyclopropylmethylsilanes - A Stereocontrolled Access to Carba-Sugars
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(200003)2000:6<995::aid-ejoc995>3.0.co;2-iopenalex-snapshot
Molecular Dynamics-Based Models Explain the Unexpected Diastereoselectivity of the Sharpless Asymmetric Dihydroxylation of Allyl D-Xylosides
inferred← citeshttps://doi.org/10.1002/(sici)1520-636x(1998)10:9<804::aid-chir5>3.0.co;2-oopenalex-snapshot
Influence of the nature and substitution of chiral 2,3-epoxy alcohol derivatives on the enantiomeric elution order on chiralcel OD column
inferred← citeshttps://doi.org/10.1002/(sici)1520-636x(1999)11:10<745::aid-chir2>3.0.co;2-wopenalex-snapshot
Catalytic asymmetric dihydroxylation of alkenes induced by polymeric chiral ligands
inferred← citeshttps://doi.org/10.1002/(sici)1520-636x(2000)12:4<256::aid-chir11>3.0.co;2-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19980202)110:3<260::aid-ange260>3.0.co;2-6openalex-snapshot
C3-Symmetrie in der asymmetrischen Katalyse und der chiralen Erkennung
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19980216)110:4<402::aid-ange402>3.0.co;2-6openalex-snapshot
Der katalytische enantioselektive Aufbau von Molekülen mit quartären Kohlenstoff-Stereozentren
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19980817)110:16<2333::aid-ange2333>3.0.co;2-xopenalex-snapshot
Olefinepoxidierung mit Methyltrioxorhenium: eine Dichtefunktionalstudie zu Energetik und Mechanismen
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19980817)110:16<2383::aid-ange2383>3.0.co;2-nopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981002)110:19<2724::aid-ange2724>3.0.co;2-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981002)110:19<2872::aid-ange2872>3.0.co;2-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981002)110:19<2879::aid-ange2879>3.0.co;2-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981217)110:24<3614::aid-ange3614>3.0.co;2-ropenalex-snapshot
Ein überraschender Festphaseneffekt: Entwicklung eines regenerierbaren, „spurlosen“ Linker-Systems für Festphasenreaktionen
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990115)111:1/2<226::aid-ange226>3.0.co;2-vopenalex-snapshot
Diastereoselektive palladiumvermittelte Synthese von vicinalen Diaminen über ein dynamisches Gleichgewicht
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990201)111:3<339::aid-ange339>3.0.co;2-eopenalex-snapshot
Möglichkeiten und Grenzen der asymmetrischen Sharpless-Aminohydroxylierung in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990401)111:7<1033::aid-ange1033>3.0.co;2-wopenalex-snapshot
Selektive Alkenoxidation mit H2O2 und einem heterogenisierten Mn-Katalysator: Epoxidierung und ein neuer Zugang zu vicinalencis-Diolen
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990503)111:9<1311::aid-ange1311>3.0.co;2-popenalex-snapshot
Enantiomerenreine cyclischetrans-1,2-Diole, -Diamine und -Aminoalkohole durch intramolekulare Pinakolkupplung planar-chiraler Mono-Cr(CO)3-Komplexe von Biarylen
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990802)111:15<2230::aid-ange2230>3.0.co;2-vopenalex-snapshot
Chemie, Biologie und medizinische Anwendungen der Glycopeptid-Antibiotika
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990903)111:17<2697::aid-ange2697>3.0.co;2-jopenalex-snapshot
Struktur und Mechanismus in der Cinchonaalkaloidchemie: Ein 50 Jahre altes Fehlkonzept wird widerlegt
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19991018)111:20<3211::aid-ange3211>3.0.co;2-xopenalex-snapshot
Atomeffiziente Oxidationen von Olefinen mit molekularem Sauerstoff: Synthese von Diolen
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000103)112:1<46::aid-ange46>3.0.co;2-popenalex-snapshot
Der Stand der Totalsynthese zu Beginn des 21. Jahrhunderts
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000117)112:2<342::aid-ange342>3.0.co;2-zopenalex-snapshot
Sauerstoff und Osmium – ein neues Paar für Dihydroxylierungen?
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000204)112:3<586::aid-ange586>3.0.co;2-#openalex-snapshot
Diastereoselektive Ce(O i Pr) 3 ‐katalysierte Pinakolkupplung von Aldehyden
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000204)112:3<591::aid-ange591>3.0.co;2-fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000218)112:4<744::aid-ange744>3.0.co;2-7openalex-snapshot
Diastereoselective Pinacol Coupling Reactions of α-Ketoamides Mediated by SmI2: Synthesis of Enantiomerically PureR andS Quaternary Tartaric Acids
inferred← citeshttps://doi.org/10.1002/(sici)1521-3765(19980515)4:5<950::aid-chem950>3.0.co;2-bopenalex-snapshot
Enantioselective Preparation of C2-Symmetrical Ferrocenyl Ligands for Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/(sici)1521-3773(20000218)39:4<728::aid-anie728>3.0.co;2-6openalex-snapshot
Diastereoselective Pinacol Coupling Reactions ofα-Ketoamides Mediated by SmI2: Synthesis of Enantiomerically PureR andS Quaternary Tartaric Acids
inferred← citeshttps://doi.org/10.1002/047084289x.rd232.pub2openalex-snapshot
Dihydroquinidine Acetate
inferred← citeshttps://doi.org/10.1002/047084289x.rd405s.pub2openalex-snapshot
1,3,2-Dioxathiolane 2,2-Dioxide
inferred← citeshttps://doi.org/10.1002/047084289x.rm216.pub2openalex-snapshot
N-MethylmorpholineN-Oxide
inferred← citeshttps://doi.org/10.1002/047084289x.rn00098openalex-snapshot
(S,S)-1,2-Diphenylethylenediamine
inferred← citeshttps://doi.org/10.1002/047084289x.rn00163openalex-snapshot
Poly(ethylene glycol)-supported 1,4-phthalazinediyl Diether Hydroquinidine ‘(DHQD)2PHAL’ Ligand
inferred← citeshttps://doi.org/10.1002/047084289x.rn00721openalex-snapshot
3,3,4,4-Tetrafluoro-4-bromo-1-butene and 3,3,4,4-tetrafluoro-4-iodo-1-butene
inferred← citeshttps://doi.org/10.1002/047084289x.rn01493openalex-snapshot
(8α,9R)-(8″α,9″R)-9,9″-[1,4-Phthalazinediylbis(oxy)]bis[10,11-dihydro-6′-methoxycinchonan] & (9S)-(9″S)-9,9″-[1,4-Phthalazinediylbis(oxy)]bis[10,11-dihydro-6′-methoxycinchonan]
inferred← citeshttps://doi.org/10.1002/047084289x.ro010.pub2openalex-snapshot
Osmium Tetroxide-Potassium Ferricyanide
inferred← citeshttps://doi.org/10.1002/0470857234.ch19openalex-snapshot
Electrophilic Additions to Double Bonds
inferred← citeshttps://doi.org/10.1002/0470862106.ia171openalex-snapshot
Osmium: Inorganic & Coordination Chemistry
inferred← citeshttps://doi.org/10.1002/0470862106.ia409openalex-snapshot
Nanostructured Catalysts: Controlling Single‐Site Composition
inferred← citeshttps://doi.org/10.1002/0471238961.1612012007090114.a01openalex-snapshot
Platinum‐Group Metals, Compounds
inferred← citeshttps://doi.org/10.1002/0471264180.or058.01openalex-snapshot
Simmons‐Smith Cyclopropanation Reaction
inferred← citeshttps://doi.org/10.1002/0471264180.or066.02openalex-snapshot
Asymmetric Dihydroxylation of Alkenes
inferred← citeshttps://doi.org/10.1002/0471264180.or067.01openalex-snapshot
Catalytic Enantioselective Aldol Addition Reactions
inferred← citeshttps://doi.org/10.1002/0471264180.or076.01openalex-snapshot
Hydrogen‐Bonding‐Mediated Directed Osmium Dihydroxylation
inferred← citeshttps://doi.org/10.1002/0471264180.or086.01openalex-snapshot
Ring‐Expanding Carbonylation of Epoxides
inferred← citeshttps://doi.org/10.1002/0471264180.or105.01openalex-snapshot
Enantioselective Halofunctionalization of Alkenes
inferred← citeshttps://doi.org/10.1002/0471264180.or108.02openalex-snapshot
Transition‐Metal‐Catalyzed Aminooxygenation of Alkenes
inferred← citeshttps://doi.org/10.1002/0471264180.or110.02openalex-snapshot
Enantioselective Epoxide Opening
inferred← citeshttps://doi.org/10.1002/0471264180.os076.10openalex-snapshot
Synthesis of Chiral Non‐Racemic Diols from (S,S)‐1,2,3,4‐Diepoxybutane: (2S,3S)‐Dihydroxy‐1,4‐Diphenylbutane
inferred← citeshttps://doi.org/10.1002/0471264229.os082.02openalex-snapshot
Preparation of Optically Active ( R , R )‐Hydrobenzoin from Benzoin or Benzil
inferred← citeshttps://doi.org/10.1002/0471264229.os094.28openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/0471264229.os095.27openalex-snapshot
Stereoretentive Iron‐catalyzed Cross‐coupling of an Enol Tosylate with MeMgBr
inferred← citeshttps://doi.org/10.1002/0471264229.os102.24openalex-snapshot
Large‐Scale Alkene Dimesyloxylation
inferred← citeshttps://doi.org/10.1002/0471266949.bmc016openalex-snapshot
Chirality and Biological Activity
inferred← citeshttps://doi.org/10.1002/1099-0690(200010)2000:20<3447::aid-ejoc3447>3.0.co;2-topenalex-snapshot
A Stereoselective Synthesis of Dihydrosphingosine
inferred← citeshttps://doi.org/10.1002/1099-0690(200011)2000:22<3703::aid-ejoc3703>3.0.co;2-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1099-0690(200105)2001:10<1873::aid-ejoc1873>3.0.co;2-oopenalex-snapshot
Total Synthesis of Korormicin
inferred← citeshttps://doi.org/10.1002/1099-0690(200105)2001:9<1769::aid-ejoc1769>3.0.co;2-dopenalex-snapshot
Substrate Binding in the Asymmetric Dihydroxylation Reaction − Investigation of the Stereoselectivity in the Dihydroxylation ofCs-Symmetric Divinylcarbinol Derivatives
inferred← citeshttps://doi.org/10.1002/1099-0690(200106)2001:11<2145::aid-ejoc2145>3.0.co;2-jopenalex-snapshot
New Enantioselective Synthesis of (10R,11S)-(+)-Juvenile Hormones I and II
inferred← citeshttps://doi.org/10.1002/1099-0690(200209)2002:17<2921::aid-ejoc2921>3.0.co;2-nopenalex-snapshot
A Concise Synthesis of (+)-Compactin Lactone by Asymmetric Dihydroxylation and Regioselective Cyclic Sulfite Opening Reactions
inferred← citeshttps://doi.org/10.1002/1520-636x(2000)12:7<581::aid-chir6>3.0.co;2-popenalex-snapshot
Total synthesis of gigantetrocin A
inferred← citeshttps://doi.org/10.1002/1521-3757(20000616)112:12<2165::aid-ange2165>3.0.co;2-jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3757(20000703)112:13<2292::aid-ange2292>3.0.co;2-vopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3757(20000717)112:14<2636::aid-ange2636>3.0.co;2-iopenalex-snapshot
Asymmetric Synthesis of Phorboxazole B—Part II: Synthesis of the C1–C19 Subunit and Fragment Assembly
inferred← citeshttps://doi.org/10.1002/1521-3757(20001117)112:22<4233::aid-ange4233>3.0.co;2-zopenalex-snapshot
A Versatile Periodate-Coupled Fluorogenic Assay for Hydrolytic Enzymes
inferred← citeshttps://doi.org/10.1002/1521-3757(20010105)113:1<205::aid-ange205>3.0.co;2-aopenalex-snapshot
A Chemical Model of Homeostasis
inferred← citeshttps://doi.org/10.1002/1521-3757(20010119)113:2<465::aid-ange465>3.0.co;2-7openalex-snapshot
Induction of a Preferred Twist in a Biphenyl Core by Stereogenic Centers: A Novel Approach to the Absolute Configuration of 1,2- and 1,3-Diols
inferred← citeshttps://doi.org/10.1002/1521-3757(20010202)113:3<606::aid-ange606>3.0.co;2-ropenalex-snapshot
A Heterogeneouscis-Dihydroxylation Catalyst with Stable, Site-Isolated Osmium-Diolate Reaction Centers
inferred← citeshttps://doi.org/10.1002/1521-3757(20010601)113:11<2056::aid-ange2056>3.0.co;2-wopenalex-snapshot
Click-Chemie: diverse chemische Funktionalität mit einer Handvoll guter Reaktionen
inferred← citeshttps://doi.org/10.1002/1521-3757(20011105)113:21<4179::aid-ange4179>3.0.co;2-#openalex-snapshot
Stereocontrolled Total Synthesis of (+)‐Altohyrtin A/Spongistatin 1
inferred← citeshttps://doi.org/10.1002/1521-3757(20011217)113:24<4755::aid-ange4755>3.0.co;2-fopenalex-snapshot
A Trifunctional Catalyst for the Synthesis of Chiral Diols
inferred← citeshttps://doi.org/10.1002/1521-3757(20011217)113:24<4849::aid-ange4849>3.0.co;2-oopenalex-snapshot
The Total Synthesis of Heliquinomycinone
inferred← citeshttps://doi.org/10.1002/1521-3757(20020201)114:3<490::aid-ange490>3.0.co;2-mopenalex-snapshot
A New Approach to Osmium-Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins
inferred← citeshttps://doi.org/10.1002/1521-3757(20020301)114:5<862::aid-ange862>3.0.co;2-7openalex-snapshot
A Novel Regio- and Stereoselective Synthesis of Sulfamidates from 1,2-Diols Using Burgess and Related Reagents: A Facile Entry intoβ-Amino Alcohols
inferred← citeshttps://doi.org/10.1002/1521-3757(20020703)114:13<2394::aid-ange2394>3.0.co;2-1openalex-snapshot
Charakterisierung einer Δ8-Sphingolipid-Desaturase aus Höheren Pflanzen: stereochemische und mechanistische Analyse zum Ursprung vonE/Z-Isomeren
inferred← citeshttps://doi.org/10.1002/1521-3765(20001117)6:22<4091::aid-chem4091>3.0.co;2-wopenalex-snapshot
A New, Non-Iterative Asymmetric Synthesis of Long-Chain 1,3-Polyols
inferred← citeshttps://doi.org/10.1002/1521-3765(20010105)7:1<72::aid-chem72>3.0.co;2-1openalex-snapshot
Towards a Correlation of Absolute Configuration and Chiroptical Properties of Alkyl Aryl Sulfoxides: A Coupled-Oscillator Foundation of the Empirical Mislow Rule?
inferred← citeshttps://doi.org/10.1002/1521-3765(20020402)8:7<1670::aid-chem1670>3.0.co;2-4openalex-snapshot
Total Synthesis of a Stereoisomer of Bistramide C and Assignment of Configuration of the Natural Product
inferred← citeshttps://doi.org/10.1002/1521-3773(20000717)39:14<2536::aid-anie2536>3.0.co;2-uopenalex-snapshot
Asymmetric Synthesis of Phorboxazole B—Part II: Synthesis of the C1-C19 Subunit and Fragment Assembly
inferred← citeshttps://doi.org/10.1002/1521-3773(20001117)39:22<4067::aid-anie4067>3.0.co;2-9openalex-snapshot
A Versatile Periodate-Coupled Fluorogenic Assay for Hydrolytic Enzymes
inferred← citeshttps://doi.org/10.1002/1521-3773(20010105)40:1<199::aid-anie199>3.0.co;2-hopenalex-snapshot
A Chemical Model of Homeostasis
inferred← citeshttps://doi.org/10.1002/1521-3773(20010119)40:2<451::aid-anie451>3.0.co;2-2openalex-snapshot
Induction of a Preferred Twist in a Biphenyl Core by Stereogenic Centers: A Novel Approach to the Absolute Configuration of 1,2- and 1,3-Diols
inferred← citeshttps://doi.org/10.1002/1521-3773(20010202)40:3<586::aid-anie586>3.0.co;2-lopenalex-snapshot
A Heterogeneous cis-Dihydroxylation Catalyst with Stable, Site-Isolated Osmium-Diolate Reaction Centers
inferred← citeshttps://doi.org/10.1002/1521-3773(20010601)40:11<2004::aid-anie2004>3.0.co;2-5openalex-snapshot
Click Chemistry: Diverse Chemical Function from a Few Good Reactions
inferred← citeshttps://doi.org/10.1002/1521-3773(20011105)40:21<4055::aid-anie4055>3.0.co;2-hopenalex-snapshot
Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1 Financial support was provided by the EPSRC (GR/L41646), Cambridge Commonwealth Trust (Scholarship to M.J.C.), EC (Marie Curie Postdoctoral Fellowship to J.L.A.), DFG (Postdoctoral Fellowship to T.T.), NSERC-Canada (Postdoctoral…
inferred← citeshttps://doi.org/10.1002/1521-3773(20011217)40:24<4619::aid-anie4619>3.0.co;2-uopenalex-snapshot
A Trifunctional Catalyst for the Synthesis of Chiral Diols
inferred← citeshttps://doi.org/10.1002/1521-3773(20011217)40:24<4713::aid-anie4713>3.0.co;2-nopenalex-snapshot
The Total Synthesis of Heliquinomycinone
inferred← citeshttps://doi.org/10.1002/1521-3773(20020201)41:3<472::aid-anie472>3.0.co;2-7openalex-snapshot
A New Approach to Osmium-Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins
inferred← citeshttps://doi.org/10.1002/1521-3773(20020301)41:5<834::aid-anie834>3.0.co;2-vopenalex-snapshot
A Novel Regio- and Stereoselective Synthesis of Sulfamidates from 1,2-Diols Using Burgess and Related Reagents: A Facile Entry into β-Amino Alcohols We thank Professor K. Barry Sharpless for the gracious donation of several of the starting diol substrates. We also thank Drs. D. H. Huang, G.…
inferred← citeshttps://doi.org/10.1002/1521-3773(20020703)41:13<2298::aid-anie2298>3.0.co;2-gopenalex-snapshot
Characterization of a Δ8-Sphingolipid Desaturase from Higher Plants: A Stereochemical and Mechanistic Study on the Origin ofE,Z Isomers
inferred← citeshttps://doi.org/10.1002/9780470048672.wecb651openalex-snapshot
Pharmaceutical Industry: Biocatalysts and Chemocatalysts
inferred← citeshttps://doi.org/10.1002/9780470166482.ch8openalex-snapshot
Metal–Carbohydrate Complexes in Solution
inferred← citeshttps://doi.org/10.1002/9780470584248.ch8openalex-snapshot
Asymmetric CarbonCarbon Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/9780470638859.conrr582openalex-snapshot
Sharpless Dihydroxylation
inferred← citeshttps://doi.org/10.1002/9780470669228.ch3openalex-snapshot
Synthesis of Insect Bioregulators Other than Pheromones
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0131openalex-snapshot
Some Synthetic Uses of Double‐Bonded Functional Groups
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0136openalex-snapshot
Electrophilic Additions to Double Bonds
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0352openalex-snapshot
Synthetic Uses of Peroxides
inferred← citeshttps://doi.org/10.1002/9780470749043.ch8openalex-snapshot
An Introduction to Diversity‐Oriented Synthesis
inferred← citeshttps://doi.org/10.1002/9780470842898.rn00721openalex-snapshot
3,3,4,4-Tetrafluoro-4-bromo-1-butene and 3,3,4,4-tetrafluoro-4-iodo-1-butene
inferred← citeshttps://doi.org/10.1002/9780470842898.rp213.pub2openalex-snapshot
Potassium Ferricyanide
inferred← citeshttps://doi.org/10.1002/9781118003497.ch5openalex-snapshot
Nanocrystalline Magnesium Oxide for Asymmetric Organic Reactions
inferred← citeshttps://doi.org/10.1002/9781118063965.ch2openalex-snapshot
Polymer‐Immobilized Chiral Organocatalyst
inferred← citeshttps://doi.org/10.1002/9781118087992.ch1openalex-snapshot
Recyclable Stereoselective Catalysts
inferred← citeshttps://doi.org/10.1002/9781118087992.ch15openalex-snapshot
Recent Advances in the Metal‐Catalyzed Stereoselective Synthesis of Biologically Active Molecules
inferred← citeshttps://doi.org/10.1002/9781118309872.ch1openalex-snapshot
Transition Metal Catalysis in the Pharmaceutical Industry
inferred← citeshttps://doi.org/10.1002/9781118571811.ch8openalex-snapshot
Metal‐Catalyzed Organic Transformations Inside a Protein Scaffold using Artificial Metalloenzymes
inferred← citeshttps://doi.org/10.1002/9781118596784.ssd022openalex-snapshot
Sulfur Dioxide: A Powerful Tool for the Stereoselective Construction of C C Bonds
inferred← citeshttps://doi.org/10.1002/9781118596784.ssd034openalex-snapshot
Transition‐Metal–Catalyzed Stereoselective Oxidations in Drug and Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/9781118662083.cot07-005openalex-snapshot
Formation of Alcohols and Phenols by Alkene, Diene, and Alkyne Additions
inferred← citeshttps://doi.org/10.1002/9781118711613.ch5openalex-snapshot
Domino and Other Olefin Metathesis Reaction Sequences
inferred← citeshttps://doi.org/10.1002/9781118940228.ch1openalex-snapshot
Principles for Synthetic Efficiency and Expansion of the Field
inferred← citeshttps://doi.org/10.1002/9781119129301.ch6openalex-snapshot
Oxidation and Reduction of Porphyrins
inferred← citeshttps://doi.org/10.1002/9781119487043.ch9openalex-snapshot
Hydrolytic and Dehydratase Enzymes
inferred← citeshttps://doi.org/10.1002/9781119663331.ch1openalex-snapshot
Total Synthesis: Some Elements to Contemplate
inferred← citeshttps://doi.org/10.1002/9781119844792.ch2openalex-snapshot
Synthesis of Epigallocatechin Gallate, Nobiletin, and Their Derivatives for Chemical‐Biological Studies
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0157openalex-snapshot
Osmium: Inorganic & Coordination Chemistry
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0350openalex-snapshot
Nanostructured Catalysts: Controlling Single‐Site Composition
inferred← citeshttps://doi.org/10.1002/9783527613144.ch10openalex-snapshot
Catalytic Heterogeneous Enantioselective Dihydroxylation and Epoxidation
inferred← citeshttps://doi.org/10.1002/9783527613182.ch6openalex-snapshot
Asymmetric Nitrogen Transfer with Nitridomanganese Complexes
inferred← citeshttps://doi.org/10.1002/9783527618231.ch3eopenalex-snapshot
Special Products: 3.3.1–3.3.6.5
inferred← citeshttps://doi.org/10.1002/9783527619351.ch3dopenalex-snapshot
Special Products: Sections 3.3.1–3.3.4
inferred← citeshttps://doi.org/10.1002/9783527619399.ch5eopenalex-snapshot
Asymmetric Dihydroxylation
inferred← citeshttps://doi.org/10.1002/9783527619399.ch5fopenalex-snapshot
Asymmetric Aminohydroxylation
inferred← citeshttps://doi.org/10.1002/9783527619405.ch5eopenalex-snapshot
Asymmetric Dihydroxylation
inferred← citeshttps://doi.org/10.1002/9783527619405.ch5fopenalex-snapshot
Asymmetric Aminohydroxylation
inferred← citeshttps://doi.org/10.1002/9783527619849.ch25openalex-snapshot
New Syntheses with Oils and Fats as Renewable Raw Materials for the Chemical Industry
inferred← citeshttps://doi.org/10.1002/9783527619962.ch10openalex-snapshot
The Sharpless Asymmetric Aminohydroxylation of Olefins
inferred← citeshttps://doi.org/10.1002/9783527620784.ch10bopenalex-snapshot
The Sharpless Asymmetric Aminohydroxylation of Olefins
inferred← citeshttps://doi.org/10.1002/9783527623013.ch7openalex-snapshot
Enantioselective Catalysis in Ionic Liquids and Supercritical CO2
inferred← citeshttps://doi.org/10.1002/9783527623235.ch9openalex-snapshot
Sulfones in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/9783527623839.ch20openalex-snapshot
Biocatalytic Asymmetric Oxidations with Oxygen
inferred← citeshttps://doi.org/10.1002/9783527627547.ch5openalex-snapshot
Design of Well‐Defined Active Sites on Crystalline Materials for Liquid‐Phase Oxidations
inferred← citeshttps://doi.org/10.1002/9783527628179.ch1openalex-snapshot
An Overview of Cinchona Alkaloids in Chemistry
inferred← citeshttps://doi.org/10.1002/9783527628179.ch12openalex-snapshot
Organic Chemistry of Cinchona Alkaloids
inferred← citeshttps://doi.org/10.1002/9783527628179.ch3openalex-snapshot
Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations
inferred← citeshttps://doi.org/10.1002/9783527628698.hgc031openalex-snapshot
Biotransformations and the Pharma Industry
inferred← citeshttps://doi.org/10.1002/9783527632039.ch1openalex-snapshot
Recent Developments in Metal‐Catalyzed Dihydroxylation of Alkenes
inferred← citeshttps://doi.org/10.1002/9783527632039.ch11openalex-snapshot
Manganese‐Catalyzed Oxidation with Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1002/9783527652235.ch46openalex-snapshot
Asymmetric Diamination of Alkenes
inferred← citeshttps://doi.org/10.1002/9783527655588.ch16openalex-snapshot
Oxidative Functionalization of Alkenes
inferred← citeshttps://doi.org/10.1002/9783527664801.ch9openalex-snapshot
An Overview of Recent Developments in Metal‐Catalyzed Asymmetric Transformations
inferred← citeshttps://doi.org/10.1002/9783527675142.ch21openalex-snapshot
Lewis Base‐Catalyzed, Lewis Acid‐Mediated Reactions ( n ?→?σ*)
inferred← citeshttps://doi.org/10.1002/9783527675906.ch12openalex-snapshot
Asymmetric Phase‐Transfer Catalysis in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/9783527681020.ch5openalex-snapshot
Hydrogen Bonding‐Mediated Cooperative Organocatalysis by Modified Cinchona Alkaloids
inferred← citeshttps://doi.org/10.1002/9783527694174.ch1openalex-snapshot
Click Chemistry: Mechanistic and Synthetic Perspectives
inferred← citeshttps://doi.org/10.1002/9783527809042.ch8openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Reactions via Azolium Enolates and Dienolates
inferred← citeshttps://doi.org/10.1002/9783527814268.ch3openalex-snapshot
One‐pot Sequential Chemoenzymatic Reactions
inferred← citeshttps://doi.org/10.1002/9783527825172.ch5openalex-snapshot
Asymmetric Synthesis of Nonbiaryl Atropisomers
inferred← citeshttps://doi.org/10.1002/9783527826131.ch10openalex-snapshot
Manganese‐Catalyzed Dihydroxylation and Epoxidation of Olefins
inferred← citeshttps://doi.org/10.1002/9783527828166.ch3openalex-snapshot
Olefination, Metathesis, and Epoxidation Reactions
inferred← citeshttps://doi.org/10.1002/9783527829569.ch12openalex-snapshot
Sustainable Methods in Hypervalent Iodine Chemistry
inferred← citeshttps://doi.org/10.1002/9783527834204.ch10openalex-snapshot
Alkaloids as Chiral Building Blocks, Auxiliaries, Ligands, and Molecular Diversity
inferred← citeshttps://doi.org/10.1002/adma.200900238openalex-snapshot
Orthogonal Transformations on Solid Substrates: Efficient Avenues to Surface Modification
inferred← citeshttps://doi.org/10.1002/adsc.200202164openalex-snapshot
Recent Advances in Asymmetric CC and C‐Heteroatom Bond Forming Reactions using Polymer‐Bound Catalysts
inferred← citeshttps://doi.org/10.1002/adsc.200202199openalex-snapshot
Microencapsulated Osmium Tetroxide‐Catalyzed Asymmetric Dihydroxylation of Olefins in Water without Using Organic Cosolvents
inferred← citeshttps://doi.org/10.1002/adsc.200303043openalex-snapshot
Efficient Osmium/Rhenium‐Catalyzed Dihydroxylation of Olefins with Hydrogen Peroxide under Acidic Conditions
inferred← citeshttps://doi.org/10.1002/adsc.200303114openalex-snapshot
Catalytic Asymmetric Dihydroxylation of Aliphatic Olefins with Reusable Resin‐Osmium Tetroxide
inferred← citeshttps://doi.org/10.1002/adsc.200303133openalex-snapshot
Achiral Dihydroxylation of Olefins by Osmate (OsO42−) Stabilised on Nanocrystalline Magnesium Oxide
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