Efficient synthesis of enantiomerically pure beta2-amino acids via chiral isoxazolidinones.
about
Pyrido[1,2-a]benzimidazole-based agents active against tuberculosis (TB), multidrug-resistant (MDR) TB and extensively drug-resistant (XDR) TBSynthesis of Fmoc-Gly-Ile Phosphinic Pseudodipeptide: Residue Specific Conditions for Construction of Matrix Metalloproteinase Inhibitor Building BlocksTriple-helical transition state analogues: a new class of selective matrix metalloproteinase inhibitors.Iterative in situ click chemistry creates antibody-like protein-capture agents.Structural and biological exploration of phe(3)-phe(4)-modified endomorphin-2 peptidomimetics.Enantioselective rhodium enolate protonations. A new methodology for the synthesis of beta2-amino acids.Direct amination of homoenolates catalyzed by N-heterocyclic carbenes.Efficient synthesis of Fmoc-protected phosphinic pseudodipeptides: Building blocks for the synthesis of matrix metalloproteinase inhibitors.Organocatalysed decarboxylative protonation process from Meldrum's acid: enantioselective synthesis of isoxazolidinones.Chiral recognition and separation of beta2-amino acids using non-covalently molecularly imprinted polymers.Asymmetric synthesis of 2-alkyl- and 2-aryl-3-aminopropionic acids (beta2-amino acids) from (S)-N-acryloyl-5,5-dimethyloxazolidin-2-one SuperQuat derivatives.A four-component reaction involving in situ generated organometallic reagents: straightforward access to β-amino esters.Enantioselective Phase-Transfer Catalyzed α-Sulfanylation of Isoxazolidin-5-ones: An Entry to β(2,2) -Amino Acid Derivatives.Quaternary β2,2 -Amino Acids: Catalytic Asymmetric Synthesis and Incorporation into Peptides by Fmoc-Based Solid-Phase Peptide Synthesis.CO- and HCl-free synthesis of acid chlorides from unsaturated hydrocarbons via shuttle catalysis.Synthesis, pharmacological evaluation and conformational investigation of endomorphin-2 hybrid analogues
P2860
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P2860
Efficient synthesis of enantiomerically pure beta2-amino acids via chiral isoxazolidinones.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
@zh-my
2003年学术文章
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2003年學術文章
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2003年學術文章
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name
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@en
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@nl
type
label
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@en
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@nl
prefLabel
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@en
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@nl
P2093
P356
P1476
Efficient synthesis of enantio ...... s via chiral isoxazolidinones.
@en
P2093
Byeong Moon Kim
Hee-Seung Lee
Jin-Seong Park
Samuel H Gellman
P304
P356
10.1021/JO026738B
P407
P577
2003-02-01T00:00:00Z