A modular synthesis of dithiocarbamate pendant unnatural α-amino acids
Published 2012 View Full Article
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Title
A modular synthesis of dithiocarbamate pendant unnatural α-amino acids
Authors
Keywords
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Journal
CHEMICAL COMMUNICATIONS
Volume 48, Issue 71, Pages 8889
Publisher
Royal Society of Chemistry (RSC)
Online
2012-06-29
DOI
10.1039/c2cc32894a
References
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Note: Only part of the references are listed.- Stereo- and regio-selective one-pot synthesis of triazole-based unnatural amino acids and β-amino triazoles
- (2012) R. B. Nasir Baig et al. CHEMICAL COMMUNICATIONS
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- (2011) Lara Mata et al. JOURNAL OF ORGANIC CHEMISTRY
- Research highlights
- (2011) NATURE BIOTECHNOLOGY
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- (2011) R.B. Nasir Baig et al. TETRAHEDRON
- Structural Chemistry of Peptides Containing Backbone Expanded Amino Acid Residues: Conformational Features of β, γ, and Hybrid Peptides
- (2010) Prema. G. Vasudev et al. CHEMICAL REVIEWS
- Synthesis of Unnatural Selenocystines and β-Aminodiselenides via Regioselective Ring-Opening of Sulfamidates Using a Sequential, One-Pot, Multistep Strategy
- (2010) Nasir Baig Rashid Baig et al. JOURNAL OF ORGANIC CHEMISTRY
- Efficient electronic coupling and improved stability with dithiocarbamate-based molecular junctions
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- Cyclic Sulfamidates as Vehicles for the Synthesis of Poly- and Diversely Substituted Benzosultams via Unusual S(O)2−O Bond Cleavage
- (2010) Magali Lorion et al. ORGANIC LETTERS
- Genetic Incorporation of Unnatural Amino Acids into Proteins in Mycobacterium tuberculosis
- (2010) Feng Wang et al. PLoS One
- Metal-Catalyzed Derivatization of Cα-Tetrasubstituted Amino Acids and Their Use in the Synthesis of Cyclic Peptides
- (2009) Andreas Grauer et al. Chemistry-An Asian Journal
- Peptidomimetics - A Versatile Route to Biologically Active Compounds
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- Facile Entry into Triazole Fused Heterocycles via Sulfamidate Derived Azido-alkynes
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- Positional Scanning for Peptide Secondary Structure by Systematic Solid-Phase Synthesis of Amino Lactam Peptides
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- One-pot copper nanoparticle-catalyzed synthesis of S-aryl- and S-vinyl dithiocarbamates in water: high diastereoselectivity achieved for vinyl dithiocarbamates
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- Catalysis by Ionic Liquids: Significant Rate Acceleration with the Use of [pmIm]Br in the Three-Component Synthesis of Dithiocarbamates
- (2007) Brindaban C. Ranu et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
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