about
Side-chain control of beta-peptide secondary structures.Synthesis of pdCpAs and transfer RNAs activated with thiothreonine and derivatives.Monoterpene-based chiral β-amino acid derivatives prepared from natural sources: syntheses and applications.α/β-Peptide foldamers: state of the art.Differentiation of isomeric amino acid residues in proteins and peptides using mass spectrometry.Highly functionalized cyclic β-amino acid moieties as promising scaffolds in peptide research and drug design.Cytotoxic activity of new racemic and optically active N-phosphonoalkyl bicyclic β-amino acids against human malignant cell lines.(3S*,4S*,E)-tert-Butyl 3,4-dibromo-5-oxo-cyclo-oct-1-ene-carboxyl-ate.Mechanochemical enzymatic resolution of N-benzylated-β3-amino estersSynthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines.Efficient regio- and stereoselective access to novel fluorinated β-aminocyclohexanecarboxylates.Synthesis of 2-substituted tryptophans via a C3- to C2-alkyl migration.Stereoselective synthesis of perillaldehyde-based chiral β-amino acid derivatives through conjugate addition of lithium amides.Improved enzymatic syntheses of valuable beta-arylalkyl-beta-amino acid enantiomers.Rh(II)-catalyzed reaction of alpha-diazocarbonyl compounds bearing beta-trichloroacetylamino substituent: C-H insertion versus 1,2-H shift.Asymmetric syntheses of enantiopure C(5)-substituted transpentacins via diastereoselective Ireland-Claisen rearrangements.A new access route to functionalized cispentacins from norbornene β-amino acids.Alkyne-azide cycloadditions with copper powder in a high-pressure continuous-flow reactor: high-temperature conditions versus the role of additives.Preparation of methyl (1R,2S,5S)- and (1S,2R,5R)-2-amino-5-tert-butyl-cyclopentane-1-carboxylates by parallel kinetic resolution of methyl (RS)-5-tert-butyl-cyclopentene-1-carboxylate.Asymmetric synthesis of (1R,2S,3R)-3-methylcispentacin and (1S,2S,3R)-3-methyltranspentacin by kinetic resolution of tert-butyl (+/-)-3-methylcyclopentene-1-carboxylate.Chiral differentiation of some cyclopentane and cyclohexane beta-amino acid enantiomers through ion/molecule reactions.Diastereochemical differentiation of some cyclic and bicyclic beta-amino acids, via the kinetic method.Direct high-performance liquid chromatographic enantioseparation of beta-lactam stereoisomers.Efficient Enzymatic Routes for the Synthesis of New Eight-membered Cyclic β-Amino Acid and β-Lactam Enantiomers.Radical-mediated nitrile translocation as the key step in the stereoselective transformation of 2-(4-chloro-2-cyanobutyl)aziridines to methyl cis-(1-arylmethyl-4-phenylpiperidin-2-yl)acetates.Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro-N-sulfinylimines.Synthesis of novel β-aminocyclobutanecarboxylic acid derivatives by a solvent-free aza-Michael addition and subsequent ring closure.Asymmetric synthesis of chloroisothreonine derivatives via syn-stereoselective Mannich-type additions across N-sulfinyl-α-chloroimines.Selective Synthesis of Fluorine-Containing Cyclic β-Amino Acid Scaffolds.Synthesis of a series of novel chiral Lewis base catalysts and their application in promoting asymmetric hydrosilylation of β-enamino esters.Diastereochemical differentiation of beta-amino acids using host-guest complexes studied by Fourier transform ion cyclotron resonance mass spectrometry.Conformational constraints in angiotensin IV to probe the role of Tyr², Pro⁵ and Phe⁶.A refined synthesis of enantiomerically pure 2-aminocyclobutanecarboxylic acids.Helical α/β-depsipeptides with alternating residue types: conformational change from the 11-helix to the 14/15-helix.Expedient synthesis of pseudo-Pro-containing peptides: towards constrained peptidomimetics and foldamersNew 1,3-amino alcohols derived from enantiopure bridgehead β-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic acidsSynthesis of new racemic and optically active N-phosphonoalkyl bicyclic β-amino acids via the kabachnik-fields reaction as potential biologically active compoundsConcise Pathway to New Multifunctionalized Constrained Pentacin Derivatives by Means of Two Stereospecific Tandem ReactionsSynthesis of enantiopure trans-N-Boc-3-aminobicyclo[2.2.2]octane-2-carboxylic acids and their bicyclic 1,3-amino alcohol derivatives via the [4+2] cycloaddition of 1,3-cyclohexadiene to a chiral β-nitroacrylate
P2860
Q35209610-72FBFA15-598C-4DE0-AA95-0E0485857B62Q36617647-FE5A4BE2-49E4-4E56-B3B6-8716A9635826Q37859312-8AD1BA41-0113-4E58-B9E0-68282B64A005Q37861031-3EA1B89E-44DE-47C9-91B4-E167DDF0FBDBQ37982946-5823A493-3572-4E01-96F0-0ACF98BF04F5Q39387421-8FAC9C86-2363-443F-8EFA-F62233885391Q39413551-F998F9F6-68A9-4C6F-9DD7-44A59224935BQ40273260-C4DAABE0-424B-4D69-805F-06B79325B802Q41469023-75C564F4-9B14-46E3-BB74-EAC0BE5746D5Q41981320-1C0C905D-3BED-4BBB-A974-31331D345156Q42239696-CB27EF5D-2658-4EF0-BDEA-4D720938E14CQ42906265-1FC7FDC1-F675-4EEA-89EC-A17AFAD5DABBQ43075307-B399CFBD-0444-433F-BCBF-5423E73FD40DQ43172235-181147FB-95E4-492D-897C-8D881121ABE2Q43219197-D327B9A0-D116-4515-AB89-D72B442B6B8AQ43415504-EA00FCFB-E1CD-4FDA-85CE-BEE1C5315E90Q43869832-E07E28AD-1A8A-4836-A936-7671C2F2F378Q44511325-A63519B3-3F9F-432C-AEA3-76E13F928FA9Q44638072-57812B07-D51C-4568-86D9-348A57EA6370Q44676433-EDDFFC61-E0E4-4F2F-ACDF-EFE31D04F1F3Q46083297-4AA98AAB-E65D-48E8-A111-4DB3AFEBDA1EQ46300191-DDB4EB84-F132-49BC-A993-FD6A05D24879Q46435874-04A99ACC-CFFA-4883-BEF1-17AB1901455CQ47253869-F46261FB-C458-4CF9-91A4-389323E24F83Q49030713-C2BBA68A-9A14-4D46-8B9C-0014FB1ADC33Q49034242-52F98854-790A-4073-B33E-28926E1C5605Q49050341-AA03E93F-DA14-447F-9064-F8B249A2913CQ49074985-18F1F497-C102-4BB9-AF34-7C7D19F32265Q50157439-EE18FFCA-C6E9-4C27-9AEC-01F6D35AB0FEQ50482039-EE1AD323-F84B-42C3-827A-EC8F70E33218Q51025335-AE77AFC8-5FAB-42D7-ABCB-5CFE4AB91B1AQ51768228-E1EE435A-E0BB-47D9-B56F-AE97EB18AAF0Q53250392-C5D2F8D2-A71C-454D-824A-E984D40CB478Q53815994-06E041F9-F08D-4B27-A627-1F41CDEA661BQ56982244-4BC7CD13-D7FE-488F-B9CA-8FF89A9327A4Q58100943-A096E925-71C2-4249-932E-4A77446EB9D6Q58101053-D9358ED9-D63A-4A3A-A5E6-CFD6476E4413Q58101178-8D7C9746-56CB-4DE7-A5CA-9AE3D8CE95DFQ58101280-FE0DC5B9-0F8D-4C35-9465-CDF38F856480
P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
The chemistry of 2-aminocycloalkanecarboxylic acids.
@ast
The chemistry of 2-aminocycloalkanecarboxylic acids.
@en
The chemistry of 2-aminocycloalkanecarboxylic acids.
@nl
type
label
The chemistry of 2-aminocycloalkanecarboxylic acids.
@ast
The chemistry of 2-aminocycloalkanecarboxylic acids.
@en
The chemistry of 2-aminocycloalkanecarboxylic acids.
@nl
prefLabel
The chemistry of 2-aminocycloalkanecarboxylic acids.
@ast
The chemistry of 2-aminocycloalkanecarboxylic acids.
@en
The chemistry of 2-aminocycloalkanecarboxylic acids.
@nl
P356
P1433
P1476
The chemistry of 2-aminocycloalkanecarboxylic acids.
@en
P2093
P304
P356
10.1021/CR000456Z
P577
2001-07-01T00:00:00Z