Pages that link to "Q56976485"
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The following pages link to Mikel Oiarbide (Q56976485):
Displaying 46 items.
- From beta-lactams to alpha- and beta-amino acid derived peptides. (Q33683261) (← links)
- Unveiling reliable catalysts for the asymmetric nitroaldol (Henry) reaction. (Q35904575) (← links)
- α-Hydroxy ketones as useful templates in asymmetric reactions. (Q38003326) (← links)
- Helical Oligourea Foldamers as Powerful Hydrogen Bonding Catalysts for Enantioselective C-C Bond-Forming Reactions (Q38645997) (← links)
- Catalytic conjugate additions of geminal bis(sulfone)s: expanding the chemistry of sulfones as simple alkyl anion equivalents. (Q43271560) (← links)
- A beta-lactam-based stereoselective access to beta,gamma-dihydroxy alpha-amino acid-derived peptides with either alpha,beta-like or unlike configurations. (Q43633140) (← links)
- Design and synthesis of a novel class of sugar-peptide hybrids: C-linked glyco beta-amino acids through a stereoselective "acetate" Mannich reaction as the key strategic element (Q44066263) (← links)
- Highly enantioselective Friedel-Crafts alkylations of pyrroles and indoles with alpha'-hydroxy enones under Cu(II)-simple bis(oxazoline) catalysis. (Q46397207) (← links)
- Enantioselective aza-Henry reactions assisted by Zn(II) and N-methylephedrine. (Q46808502) (← links)
- Catalytic enantioselective aza-Henry reaction with broad substrate scope. (Q46848925) (← links)
- Asymmetric Assembly of All-Carbon Tertiary/Quaternary Nonadjacent Stereocenters through Organocatalytic Conjugate Addition of α-Cyanoacetates to a Methacrylate Equivalent. (Q48129484) (← links)
- Catalytic Asymmetric Synthesis of Quaternary Barbituric Acids (Q48204588) (← links)
- Enantioselective Synthesis of Quaternary Δ4 - and Δ5 -Dehydroprolines Based on a Two-Step Formal [3 2] Cycloaddition of α-Aryl and α-Alkyl Isocyano(thio)acetates with Vinyl Ketones. (Q48328152) (← links)
- Bifunctional Brønsted Base Catalyst Enables Regio-, Diastereo-, and Enantioselective Cα -Alkylation of β-Tetralones and Related Aromatic-Ring-Fused Cycloalkanones. (Q48341944) (← links)
- Controlling the α/γ-Reactivity of Vinylogous Ketone Enolates in Organocatalytic Enantioselective Michael Reactions. (Q48358985) (← links)
- α-Hydroxy Ketones as Masked Ester Donors in Brønsted Base Catalyzed Conjugate Additions to Nitroalkenes (Q49988172) (← links)
- Base-Catalyzed Asymmetric α-Functionalization of 2-(Cyanomethyl)azaarene N-Oxides Leading to Quaternary Stereocenters (Q50873118) (← links)
- Catalytic enantioselective quick route to aldol-tethered 1,6- and 1,7-enynes from ω-unsaturated aldehydes. (Q51046793) (← links)
- Enantioselective Synthesis of 5,5-Disubstituted Hydantoins by Brønsted Base/H-Bond Catalyst Assisted Michael Reactions of a Design Template. (Q52633588) (← links)
- A strategy for the asymmetric aminohomologation of alpha, beta-dihydroxy aldehydes: application to the synthesis of the southwest tripeptide segment of echinocandin B. (Q53911874) (← links)
- Catalytic Enantioselective Synthesis of N,C(α),C(α)-Trisubstituted α-Amino Acid Derivatives Using 1H-Imidazol-4(5H)-ones as Key Templates. (Q54101571) (← links)
- A concise synthesis of α-amino acid N-carboxy anhydrides of (2S,3S)-β-substituted serines (Q57974613) (← links)
- Practical Synthesis of α-Amino AcidN-Carboxy Anhydrides of Polyhydroxylated α-Amino Acids from β-Lactam Frameworks. Model Studies toward the Synthesis of Directly Linked Peptidyl Nucleoside Antibiotics (Q57974615) (← links)
- Camphor-based alpha-bromo ketones for the asymmetric darzens reaction (Q73375487) (← links)
- alpha-Oxymethyl Ketone Enolates for the Asymmetric Mannich Reaction. From Acetylene and N-Alkoxycarbonylimines to beta-Amino Acids This work was supported by the University of the Basque Country, the Basque Government (Projects UPV 170.215-G47/98, E (Q73666821) (← links)
- Asymmetric synthesis of beta-mercapto carboxylic acid derivatives by intramolecular sulfur transfer in N-enoyl oxazolidine-2-thiones promoted by Lewis acids (Q73964811) (← links)
- Alkylation of chiral alpha-hydroxy ketones derived from (1R)-( )-camphor. An asymmetric variant of the classical acetylene route to carbonyl compounds (Q74607750) (← links)
- A Concise beta-Lactam Route to Short Peptide Segments Containing beta,beta-Disubstituted beta-Amino Acids (Q74837772) (← links)
- Highly Diastereoselective Aldol Reactions with Camphor-Based Acetate Enolate Equivalents (Q77052242) (← links)
- The aldol addition reaction: an old transformation at constant rebirth (Q77581900) (← links)
- Intramolecular sulfur transfer in N-enoyl oxazolidine-2-thiones promoted by Brønsted acids. Practical asymmetric synthesis of beta-mercapto carboxylic acids and mechanistic insights (Q79373484) (← links)
- Construction of C--S bonds with a quaternary stereocenter through a formal michael reaction: asymmetric synthesis of tertiary thiols (Q80234635) (← links)
- Catalytic enantioselective conjugate addition of carbamates (Q80391231) (← links)
- Lewis acid catalyzed asymmetric cycloadditions of nitrones: alpha'-hydroxy enones as efficient reaction partners (Q81149921) (← links)
- Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: stereoselective access to all-carbon quaternary centers (Q81371421) (← links)
- Enantioselective henry reactions under dual Lewis acid/amine catalysis using chiral amino alcohol ligands (Q81744767) (← links)
- Copper-catalyzed enantioselective conjugate addition of dialkylzinc reagents to alpha'-oxy enones (Q81814886) (← links)
- Enantio- and diastereoselective organocatalytic α-alkylation of aldehydes with 3-substituted 2-(bromomethyl)acrylates (Q82780626) (← links)
- Highly enantioselective conjugate additions of aldehydes to vinyl sulfones (Q83146219) (← links)
- Conjugate addition of nitroalkanes to an acrylate equivalent. Stereocontrol at C-alpha of the nitro group through double catalytic activation (Q84370437) (← links)
- Towards Direct Mukaiyama‐Type Reactions Catalytic in Silicon (Q84535742) (← links)
- Enantioselective construction of tetrasubstituted stereogenic carbons through Brønsted base catalyzed michael reactions: α'-hydroxy enones as key enoate equivalent (Q86052189) (← links)
- N-(Diazoacetyl)oxazolidin-2-thiones as sulfur-donor reagents: asymmetric synthesis of thiiranes from aldehydes (Q87378631) (← links)
- Development of a syn-Selective Mannich Reaction of Aldehydes with Propargylic Imines by Dual Catalysis: Asymmetric Synthesis of Functionalized Propargylic Amines (Q87488825) (← links)
- Enantioselective Addition of Alkynyl Ketones to Nitroolefins Assisted by Brønsted Base/H-Bonding Catalysis (Q91084435) (← links)
- Brønsted Base Catalyzed One-Pot Synthesis of Stereodefined Six-Member Carbocycles Featuring Transient Trienolates and a Key Intramolecular 1,6-Addition (Q92330555) (← links)