Amino acidic scaffolds bearing unnatural side chains: an old idea generates new and versatile tools for the life sciences
about
Oxidative diversification of amino acids and peptides by small-molecule iron catalysisSynthesis of constrained analogues of tryptophan.The Cysteine S-Alkylation Reaction as a Synthetic Method to Covalently Modify Peptide Sequences.Chemo- and Stereoselective Transition-Metal-Free Amination of Amides with Azides.Development of a protease-resistant reporter to quantify BCR-ABL activity in intact cells.Pseudomonas fluorescens Strain R124 Encodes Three Different MIO Enzymes.Uncatalysed diaryldiazo cyclopropanations on bicyclic lactams: access to annulated prolines.Reversing Polarity: Carbonyl α-Aminations with Nitrogen Nucleophiles.Ribosomal incorporation of backbone modified amino acids via an editing-deficient aminoacyl-tRNA synthetase.Practical Alkoxythiocarbonyl Auxiliaries for Iridium(I)-Catalyzed C-H Alkylation of Azacycles.Selective alkylation/oxidation of N-substituted isoindolinone derivatives: synthesis of N-phthaloylated natural and unnatural α-amino acid analogues.Unnatural Amino Acid Derivatives through Click Chemistry: Synthesis of Triazolylalanine Analogues.Chemical space screening around Phe3 in opioid peptides: Modulating µ versus δ agonism by Suzuki-Miyaura cross-couplings.Stereoselective Synthesis of β-(5-Arylthiazolyl) α-Amino Acids and Use in Neurotensin Analogues
P2860
Q28817191-54E756E0-3173-4E4A-A0D2-F17358E3590FQ35868107-3970FADC-29C1-46AF-813D-A729C3A445EBQ38931075-77E50438-3311-4D50-8EBC-1713472C1C52Q41875422-4C25A5C9-2F92-4BB4-8C27-4AA8CBBD363AQ42367946-25127D5B-4C55-40FD-ACE1-6547901C1634Q47174569-336F2A27-3280-4686-8668-99DBDF9B4322Q47704809-19B505D4-7D14-4231-A1E6-8DCA8A8C8420Q48093310-43E400A3-9B22-4415-8B84-DFC8F8440D75Q48171005-09998119-FBCE-4E93-BF91-FE3FB5BE7FE2Q48268047-8393AA68-C2C4-4218-A5C6-505C8BC7B516Q49918742-FB40BEAF-0A08-4520-A911-C13D3DF1CC0FQ55057700-DE202AF5-C286-4676-9EA2-C092F9D0F37AQ55642173-B07FDD6F-C933-4E9C-A028-FA3F3324E7E8Q58099616-DC5E39F6-3D64-43C4-8A5C-D30B7F457094
P2860
Amino acidic scaffolds bearing unnatural side chains: an old idea generates new and versatile tools for the life sciences
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Amino acidic scaffolds bearing ...... le tools for the life sciences
@ast
Amino acidic scaffolds bearing ...... le tools for the life sciences
@en
Amino acidic scaffolds bearing ...... le tools for the life sciences
@nl
type
label
Amino acidic scaffolds bearing ...... le tools for the life sciences
@ast
Amino acidic scaffolds bearing ...... le tools for the life sciences
@en
Amino acidic scaffolds bearing ...... le tools for the life sciences
@nl
prefLabel
Amino acidic scaffolds bearing ...... le tools for the life sciences
@ast
Amino acidic scaffolds bearing ...... le tools for the life sciences
@en
Amino acidic scaffolds bearing ...... le tools for the life sciences
@nl
P2093
P1476
Amino acidic scaffolds bearing ...... le tools for the life sciences
@en
P2093
Andrea Stevenazzi
Barbara Vergani
Giovanni Sandrone
Maria Lattanzio
Mattia Marchini
P304
P356
10.1016/J.BMCL.2014.10.016
P407
P577
2014-12-01T00:00:00Z