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Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinones
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Asymmetric Cycloadditions, Diels-Alder and Cyclopropanation Transformations, with (S)-Benzyl N-2-Trifluoroacetamidoacrylyl Oxazolidinone
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199803)1998:3<501::aid-ejoc501>3.0.co;2-qopenalex-snapshot
Dramatic Diastereoselectivity Differences in the Asymmetric Ene Reactions of Triazolinediones and Singlet Oxygen with Chiral 2,2-Dimethyloxazolidine Derivatives of Tiglic Acid
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Synthesis of Enantiomerically Puretrans-1,2-Disubstituted Cyclopentanes and Cyclohexanes by Intramolecular Allylsilane Addition to Chiral Alkylidene-1,3-dicarbonyl Compounds
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Stereoselective Inter- and Intramolecular Pauson–Khand Reactions ofN-(2-Alkynoyl) Derivatives of Chiral Oxazolidin-2-ones
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Polymer-supported chiral diol as ligand of Ti(IV) for enantioselective Diels-Alder reaction
inferred← citeshttps://doi.org/10.1002/047084289x.rb066mopenalex-snapshot
(S)-4-Benzyl-2-oxazolidinone
inferred← citeshttps://doi.org/10.1002/047084289x.rb066m.pub2openalex-snapshot
(S)-4-Benzyl-2-oxazolidinone
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Ethylaluminum Dichloride
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(S)-(+)-5,5-Dimethyl-4-phenyl-2-oxazolidinone
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Zirconium Tetrachloride
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Catalytic Asymmetric Ketene [2 + 2] and [4 + 2] Cycloadditions
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Enantioselective, Catalytic D iels‐ A lder Reaction: (1S‐endo)‐3‐(Bicyclo[2.2.1]Hept‐5‐en‐2‐ylcarbonyl)‐2‐Oxazolidinone
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Catalysis of Diels–Alder Reactions in Water and in Hydrogen‐Bonding Environments
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07517openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.19941060915openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.19961080821openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.199303361openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200701365openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200704830openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201102037openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201102405openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201910898openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cber.19961291108openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.19950010807openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.198823097openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.200021266openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.200900385openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.202300141openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jccs.199200013openalex-snapshot
Enantioselective Addition of Iodine Azide to α,β‐Unsaturated Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/jccs.199600030openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jccs.199700043openalex-snapshot
One‐Pot Formation of Carbonates from the Reactions of Carbonyl Compounds with Samarium Diiodide and Methyl Chloroformate
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inferred← citeshttps://doi.org/10.1002/jlac.1990199001127openalex-snapshot
Aminosäureester als chirale Hilfsgruppen in Lewis‐Säure‐katalysierten Diels‐Alder‐Reaktionen
inferred← citeshttps://doi.org/10.1002/jlac.1995199506140openalex-snapshot
Chelation control by a second nitrogen atom in formal hetero Diels‐Alder reactions of N‐arylimines
inferred← citeshttps://doi.org/10.1002/jlac.1995199511271openalex-snapshot
Molecular switches: Calculations on the stereodivergent hetero Diels‐Alder reaction of chiral 1‐oxa‐1,3‐butadienes with different lewis acids
inferred← citeshttps://doi.org/10.1002/jlac.199719970104openalex-snapshot
New Synthetic Pathways to Nitrogen Heterocycles
inferred← citeshttps://doi.org/10.1002/jlac.199719970314openalex-snapshot
Diastereoselective Synthesis of 1‐Hydroxy‐Substituted Benzo[b]quinolidines and 11‐Hydroxy‐Substituted Azepino[1,2‐b]isoquinolines via Hetero‐Ene Cyclization
inferred← citeshttps://doi.org/10.1002/jlcr.2580290604openalex-snapshot
The synthesis of (5R)‐ and (5S)‐[5‐3H]‐L‐ornithine
inferred← citeshttps://doi.org/10.1002/poc.1089openalex-snapshot
Asymmetric biomimetic oxidations of phenols using oxazolidines as chiral auxiliaries: the enantioselective synthesis of (+)‐ and (−)‐dehydrodiconiferyl alcohol
inferred← citeshttps://doi.org/10.1002/poc.828openalex-snapshot
Dual enantioselective Diels–Alder process in the cyclization of chiral acrylamide with dienes
inferred← citeshttps://doi.org/10.1002/tcr.201402058openalex-snapshot
Reductive Umpolung Reactions with Low-Valent Titanium Catalysts
inferred← citeshttps://doi.org/10.1007/2789_2007_066openalex-snapshot
Organocatalytic Syntheses of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1007/7081_2020_36openalex-snapshot
Oxazolidinones and Related Heterocycles as Chiral Auxiliaries/Evans and Post-Evans Auxiliaries
inferred← citeshttps://doi.org/10.1007/978-3-319-20544-1_4openalex-snapshot
Introduction to the Development of a Catalytic Asymmetric Synthesis of Tertiary α-Aryl Ketones
inferred← citeshttps://doi.org/10.1007/978-3-319-29454-4_2openalex-snapshot
Reactions Involving Maleic Anhydride
inferred← citeshttps://doi.org/10.1007/978-3-319-30073-3_16openalex-snapshot
Heterocyclic Synthesis Through C-N Bond Formation with Carbon Dioxide
inferred← citeshttps://doi.org/10.1007/bf01435789openalex-snapshot
On the mechanism of the Fe(CO)5-catalyzed Kharasch reaction
inferred← citeshttps://doi.org/10.1007/bf02496131openalex-snapshot
Diastereoselective bromination of(R)-N-cinnamoyl-4-phenyloxazolidin-2-one in the presence of Lewis acids
inferred← citeshttps://doi.org/10.1007/bf03246110openalex-snapshot
Some applications of zirconium(IV) tetrachloride (ZrCl4) and zirconium(IV) oxydichloride octahydrate (ZrOCl2.8H2O) as catalysts or reagents in organic synthesis
inferred← citeshttps://doi.org/10.1007/bf03246171openalex-snapshot
Zirconyl triflate, [ZrO(OTf)2], as a new and highly efficient catalyst for ring-opening of epoxides
inferred← citeshttps://doi.org/10.1007/s00706-010-0310-8openalex-snapshot
Highly efficient and selective methoxymethylation of alcohols and phenols catalyzed by reusable ZrO(OTf)2 under solvent-free conditions
inferred← citeshttps://doi.org/10.1007/s00726-014-1764-5openalex-snapshot
Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations
inferred← citeshttps://doi.org/10.1007/s00894-023-05665-7openalex-snapshot
A molecular electron density theory study of asymmetric Diels–Alder [4 + 2] reaction’s mechanism of furan with three substituted alkynes (5-R substituted-3-(3-(phenylsulfonyl)-propioloyl)-oxazolidin-2-one)
inferred← citeshttps://doi.org/10.1007/s10593-023-03203-0openalex-snapshot
Asymmetric synthesis of pyroglutamic acids via Ni(II) complex methodology
inferred← citeshttps://doi.org/10.1007/s10600-010-9531-7openalex-snapshot
Stereoselective synthesis of an alarm pheromone of Grematogaster ants using (4S)-4-benzyloxazolidinone as chiral auxiliary
inferred← citeshttps://doi.org/10.1007/s10600-010-9636-zopenalex-snapshot
Stereoselective synthesis of the sex pheromone of the yellow mealworm using (S)-4-benzyloxazolidinone as chiral auxiliary
inferred← citeshttps://doi.org/10.1007/s10947-008-0144-yopenalex-snapshot
Camphor-based α-bromoketones for the asymmetric darzens reaction: Insights into the mechanism using density functional theory
inferred← citeshttps://doi.org/10.1007/s11164-015-2260-6openalex-snapshot
A review on green Lewis acids: zirconium(IV) oxydichloride octahydrate (ZrOCl2·8H2O) and zirconium(IV) tetrachloride (ZrCl4) in organic chemistry
inferred← citeshttps://doi.org/10.1016/0022-328x(90)85218-nopenalex-snapshot
Developing potentially useful organometallic Lewis acid catalysts: (η-cyclopentadienyl)zirconium trichloride derivatives
inferred← citeshttps://doi.org/10.1016/0040-4020(92)80025-bopenalex-snapshot
Use of 1,3-oxazolidin-2-one derivatives of 3-borylpropenoic acids as β-hydroxy acrylic acid equivalents in the asymmetric Diels-Alder reaction catalyzed by a chiral titanium reagent
inferred← citeshttps://doi.org/10.1016/0040-4020(94)00940-vopenalex-snapshot
X=Y−ZH compounds as potential 1,3-dipoles. Part 43. Metal ion catalysed asymmetric 1,3-dipolar cycloaddition reactions of imines and menthyl acrylate
inferred← citeshttps://doi.org/10.1016/0040-4020(94)01140-uopenalex-snapshot
Zirconocene-catalyzed cationic Diels-Alder reactions
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00267-copenalex-snapshot
Asymmetric intramolecular Diels-Alder reactions of sulfoximine-activated trienes
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00808-3openalex-snapshot
Synthesis of β,γ-unsaturated N-acyl-2-oxazolidinones
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00826-5openalex-snapshot
Synthesis of β,γ-unsaturated N-acyl-2-oxazolidinones
inferred← citeshttps://doi.org/10.1016/0040-4039(90)80164-hopenalex-snapshot
Cleavage of N-acyl oxazolidones
inferred← citeshttps://doi.org/10.1016/0040-4039(91)80171-2openalex-snapshot
Generation of nitrile oxides through O-metalation of hydroximoyl chlorides. Chelation-controlled syn-selective cycloaddition of nitrile oxides to α-substituted allyl alcohols
inferred← citeshttps://doi.org/10.1016/0040-4039(91)80573-oopenalex-snapshot
Conformationally rigid chiral [4+2]cycloadduct-based 2-oxazolidinones as new auxiliaries
inferred← citeshttps://doi.org/10.1016/0040-4039(91)80821-mopenalex-snapshot
Asymmetric induction at two contiguous stereogenic centers by diastereoface differentiating nucleophilic addition reaction
inferred← citeshttps://doi.org/10.1016/0040-4039(94)85088-7openalex-snapshot
Exploiting steric shielding: Tuning terpenoid-derived oxazolidin-2-ones as chiral auxiliaries for the Diels-Alder reaction
inferred← citeshttps://doi.org/10.1016/0040-4039(94)85339-8openalex-snapshot
Dispiroketals in synthesis (Part 13): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective diels-alder reactions using a bifunctional, C2- symmetrical chiral auxiliary
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00560-yopenalex-snapshot
A concise synthesis of (−)-Dihydroprotolichesterinic acid via consecutive stereocontrolled 1,4-conjugate addition and syn-aldol condensation reactions
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01584-5openalex-snapshot
Highly diastereoselective diels-alder reaction mediated by a chiral auxiliary derived from amino indanol: The role of conformation on diastereoselectivity
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01984-popenalex-snapshot
A new chiral oxazolidinone derived from diphenylalaninol. Aldol, alkylation, and diels-alder reactions
inferred← citeshttps://doi.org/10.1016/0040-4039(95)02040-3openalex-snapshot
Chiral dienamides- substrates for asymmetric synthesis of amido cyclohexenes
inferred← citeshttps://doi.org/10.1016/0040-4039(95)02089-6openalex-snapshot
Highly efficient diastereoselective Exo Diels-Alder reactions of homochiral 2-(N-acylamino)-1-thia-1,3-dienes: A powerful entry into optically pure thiopyrans
inferred← citeshttps://doi.org/10.1016/0040-4039(96)00904-5openalex-snapshot
Silyloxy-cope rearrangement of chiral aldol adducts
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01284-1openalex-snapshot
Palladium-catalyzed asymmetric 1,3-dipolar cycloaddition of nitrones to olefins
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01815-1openalex-snapshot
The preparation and first application of a polymer-supported “Evans” oxazolidinone
inferred← citeshttps://doi.org/10.1016/0957-4166(94)00347-eopenalex-snapshot
Resolution of racemic carboxylic and sulfonic acids via D-xylose derived new cyclic carbamate reagents (oxazolidin-2-ones)
inferred← citeshttps://doi.org/10.1016/0957-4166(95)00087-6openalex-snapshot
An asymmetric route to the 5,6-dihydro-4H-1,3-thiazine skeleton via an asymmetric hetero diels-alder reaction
inferred← citeshttps://doi.org/10.1016/0957-4166(95)00092-4openalex-snapshot
Highly stereoselective formation of optically pure 2,4-oxazolidinedione via diastereoselective dihydroxylation of (4S)-3-((E)-3′-substituted-2′-propenoyl)-4-isopropyl-2-oxazolidinone
inferred← citeshttps://doi.org/10.1016/0957-4166(95)00139-gopenalex-snapshot
Synthesis and reactivity of enantiomerically pure N-acylN-alkyl p-toluenesulfinamides
inferred← citeshttps://doi.org/10.1016/0957-4166(95)00377-0openalex-snapshot
Synthesis and use of enantiomerically pure tert-leucine
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00010-9openalex-snapshot
Asymmetric Diels-Alder reaction: Cis-1-arylsulfonamido-2-indanols as highly effective chiral auxiliaries
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00052-3openalex-snapshot
D-xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective alkylations
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00344-8openalex-snapshot
Enantioselective Diels-Alder reactions catalyzed by chiral magnesium lewis acids prepared from hydroxysulfoxides
inferred← citeshttps://doi.org/10.1016/0960-894x(96)00015-7openalex-snapshot
Design and synthesis of ring-constrained boropeptide thrombin inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-08-034712-7.50006-0openalex-snapshot
The Diels-Alder Reaction - General Aspects
inferred← citeshttps://doi.org/10.1016/b978-0-08-034712-7.50008-4openalex-snapshot
Intramolecular Diels-Alder Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-08-044860-2.00006-4openalex-snapshot
Cycloadditions and Rearrangements
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00123-2openalex-snapshot
The Paterno–Büchi Reaction
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00128-1openalex-snapshot
Intermolecular Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00131-1openalex-snapshot
Intramolecular Diels–Alder Reactions
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