Results 101 to 110 of about 140,419 (292)
Halogenation effects in Intramolecular Furan Diels-Alder reactions:broad scope synthetic and computational studies [PDF]
For the first time a comprehensive synthetic and computational study of the effect of halogen substitution on both furan and dienophile for the intramolecular Furan Diels-Alder (IMDAF) reaction has been undertaken.
Bebbington, Magnus William Paul+3 more
core +1 more source
The regioselective three-component condensation of azomethine ylides derived from isatins and α-amino acids with acrylamides or aroylacrylic acids as dipolarophiles has been realized through a one-pot 1,3-dipolar cycloaddition protocol.
Tatyana L. Pavlovskaya+6 more
doaj +1 more source
Extracellular vesicles (EVs) are functionalized and used as crosslinkers to construct hydrogels, compatible with common crosslinking chemistries in biomaterial scaffolds. EV crosslinkers provided stress relaxation properties, promoting cell growth. They also enabled efficient protein delivery while maintaining biological activity, as VEGF‐loaded EV ...
Lufeng Shi+14 more
wiley +1 more source
Isolation of bis(copper) key intermediates in Cu-catalyzed azide-alkyne "click reaction". [PDF]
The copper-catalyzed 1,3-dipolar cycloaddition of an azide to a terminal alkyne (CuAAC) is one of the most popular chemical transformations, with applications ranging from material to life sciences.
Bertrand, Guy+3 more
core +2 more sources
The 7‐mer peptide motifs QFFLFFQ, QFFEFFQ, and QFQQSFF, known as good, medium, and poor binders for the photosensitizers m‐THPC and Chlorin E6 are covalently immobilized on commercial amino‐functionalized silica particles by inverse electron‐demand Diels‐Alder ligation.
Steffen A. Busche+5 more
wiley +1 more source
Preparation of 4 '-spirocyclobutyl nucleoside analogues as novel and versatile adenosine scaffolds
Despite the large variety of modified nucleosides that have been reported, the preparation of constrained 4 '-spirocyclic adenosine analogues has received very little attention.
De Vleeschouwer, Freija+10 more
core +1 more source
Abstract The demonstrated light‐initiated addition of radicals formed on an active methylene group to styrene derivatives exhibits a product selectivity influenced by the presence of a protic solvent. Under protic conditions, the predominant products are branched compounds with the alkene moiety attached to the methylene group.
Małgorzata Pałyga+2 more
wiley +1 more source
Abstract The use of stable photosensitizers made on a multigram‐scale from cheap and available starting materials offers an extraordinary opportunity to translate small‐scale proof‐of‐concept photoreactions to widespread applications in non‐specialized laboratories, thereby promoting the implementation of light‐driven syntheses.
Steven Sittel+5 more
wiley +1 more source
Regioselective reactions of 3,4-pyridynes enabled by the aryne distortion model. [PDF]
The pyridine heterocycle continues to play a vital role in the development of human medicines. More than 100 currently marketed drugs contain this privileged unit, which remains highly sought after synthetically. We report an efficient means to access di-
Garg, Neil K, Goetz, Adam E
core
Synthetic and computational studies on the tricarboxylate core of 6,7-dideoxysqualestatin H5 involving a carbonyl ylide cycloaddition–rearrangement [PDF]
Reaction of diazodiketoesters 17 and 28 with methyl glyoxylate in the presence of catalytic rhodium(II) acetate generates predominantly the 6,8-dioxabicyclo[3.2.1]octanes 29 and 30, respectively.
Adamo+57 more
core +1 more source