Nonnatural amino acid synthesis by using carbon-hydrogen bond functionalization methodology
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Coordinating activation strategy for C(sp(3))-H/C(sp(3))-H cross-coupling to access β-aromatic α-amino acidsVisible-light photoredox synthesis of unnatural chiral α-amino acids.Stereoselective alkoxycarbonylation of unactivated C(sp3)-H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis.Pd-catalysed ligand-enabled carboxylate-directed highly regioselective arylation of aliphatic acids.Catalytic functionalization of C(sp2)-H and C(sp3)-H bonds by using bidentate directing groups.Asymmetric palladium-catalyzed directed intermolecular fluoroarylation of styrenes.N-Heterocyclic Carbene Ligand-Enabled C(sp(3))-H Arylation of Piperidine and Tetrahydropyran Derivatives.Palladium-Catalyzed Transformations of Alkyl C-H Bonds.Ligand-Enabled Arylation of γ-C-H Bonds.Bidentate, monoanionic auxiliary-directed functionalization of carbon-hydrogen bondsLigand-enabled β-C-H arylation of α-amino acids using a simple and practical auxiliary.Mild palladium-catalyzed C-H alkylation using potassium alkyltrifluoroborates in combination with MnF3Palladium-Catalyzed Directed C(sp(3))-H Arylation of Saturated Heterocycles at C-3 Using a Concise Optimization ApproachLigand-promoted alkylation of C(sp3)-H and C(sp2)-H bonds.Palladium-catalyzed ligand-promoted site-selective cyanomethylation of unactivated C(sp3)-H bonds with acetonitrile.Scope and limitations of auxiliary-assisted, palladium-catalyzed arylation and alkylation of sp2 and sp3 C-H bonds.Synthesis and SARs of indole-based α-amino acids as potent HIV-1 non-nucleoside reverse transcriptase inhibitors.Ligand-controlled C(sp³)-H arylation and olefination in synthesis of unnatural chiral α-amino acids.Site-selective C(sp3)-H functionalization of di-, tri-, and tetrapeptides at the N-terminus.Use of a readily removable auxiliary group for the synthesis of pyrrolidones by the palladium-catalyzed intramolecular amination of unactivated γ C(sp(3))-H bonds.ω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor.8-Aminoquinoline: a powerful directing group in metal-catalyzed direct functionalization of C-H bonds.C-H bond arylation in the synthesis of aryltetralin lignans: a short total synthesis of podophyllotoxin.Palladium-catalyzed direct functionalization of 2-aminobutanoic acid derivatives: application of a convenient and versatile auxiliary.Merging organocatalysis with transition metal catalysis and using O2 as the oxidant for enantioselective C-H functionalization of aldehydes.Divergent and Stereoselective Synthesis of β-Silyl-α-Amino Acids through Palladium-Catalyzed Intermolecular Silylation of Unactivated Primary and Secondary C-H Bonds.Synthesis of unnatural α-amino acid derivatives via selective o-C-H functionalization.Sulfur-directed carbon-sulfur bond cleavage for Rh-catalyzed regioselective alkynylthiolation of alkynes.Ligand-Enabled β-C-H Arylation of α-Amino Acids Without Installing Exogenous Directing Groups.Phenyltrimethylammonium Salts as Methylation Reagents in the Nickel-Catalyzed Methylation of C-H Bonds.Resolving a Reactive Organometallic Intermediate from Dynamic Directing Group Systems by Selective C-H Activation.Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3 )-H Activation.One-pot synthesis of quaternary carbon centered cyclobutanes via Pd(ii)-catalyzed cascade C(sp3)-H activations.Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)-Catalyzed C-H Activation.Palladium-catalyzed intermolecular amination of unactivated C(sp3)-H bonds via a cleavable directing group.Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp3)-H bonds.Readily Removable Directing Group Assisted Chemo- and Regioselective C(sp(3))-H Activation by Palladium Catalysis.An NHC-catalyzed in situ activation strategy to β-functionalize saturated carboxylic acid: an enantioselective formal [3+2] annulation for spirocyclic oxindolo-γ-butyrolactones.Nickel-catalyzed chelation-assisted direct arylation of unactivated C(sp3)-H bonds with aryl halides.Direct borylation of primary C-H bonds in functionalized molecules by palladium catalysis.
P2860
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P2860
Nonnatural amino acid synthesis by using carbon-hydrogen bond functionalization methodology
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Nonnatural amino acid synthesi ...... functionalization methodology
@en
Nonnatural amino acid synthesi ...... functionalization methodology
@nl
type
label
Nonnatural amino acid synthesi ...... functionalization methodology
@en
Nonnatural amino acid synthesi ...... functionalization methodology
@nl
prefLabel
Nonnatural amino acid synthesi ...... functionalization methodology
@en
Nonnatural amino acid synthesi ...... functionalization methodology
@nl
P2860
P356
P1476
Nonnatural amino acid synthesi ...... functionalization methodology
@en
P2093
Ly Dieu Tran
Olafs Daugulis
P2860
P304
P356
10.1002/ANIE.201200731
P407
P577
2012-04-12T00:00:00Z