Amanote Research
Register
Sign In
Tandem Azide Conjugate Addition –Click Chemistry : Scope and Limitations
doi 10.3390/ecsoc-11-01316
Full Text
Open PDF
Abstract
Available in
full text
Date
November 30, 2007
Authors
Rodolfo Lavilla
Nicolas Isambert
Federica Catti
Mª-José Arévalo
Ricardo Salazar
Publisher
MDPI
Related search
Labeling Live Cells by Copper-Catalyzed Alkyne−Azide Click Chemistry
Bioconjugate Chemistry
Organic Chemistry
Biotechnology
Pharmacology
Pharmaceutical Science
Bioengineering
Biomedical Engineering
Cu Catalyzed Azide-Alkyne Cycloaddition With Pharmacological Applications of Click Chemistry
International Journal for Research in Applied Science and Engineering Technology
Scope and Limitations of Infra-Red Measurements in Chemistry
Nature
Multidisciplinary
Tandem Enantioselective Conjugate Addition−Cyclopropanation. Application to Natural Products Synthesis.
Journal of Organic Chemistry
Organic Chemistry
Design, Syntheses, and Anti-Tb Activity of 1,3-Benzothiazinone Azide and Click Chemistry Products Inspired by BTZ043
Combined CuI-catalysed Alkyne–azide Cycloaddition and Furan–maleimide Diels–Alder “Click” Chemistry Approach to Thermoresponsive Dendrimers
Chemical Communications
Surfaces
Alloys
Materials Chemistry
Coatings
Metals
Optical
Magnetic Materials
Films
Catalysis
Chemistry
Electronic
Composites
Ceramics
Tandem Asymmetric Conjugate Addition/a-Alkylation Using (S, S)-(+)-Pseudoephedrine as Chiral Auxiliary
Enantioselective Synthesis of Tryptophan Derivatives by a Tandem Friedel–Crafts Conjugate Addition/Asymmetric Protonation Reaction
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Metal-Catalyzed Azide-Alkyne “Click” Reactions: Mechanistic Overview and Recent Trends
Coordination Chemistry Reviews
Inorganic Chemistry
Materials Chemistry
Theoretical Chemistry
Physical