Results 151 to 160 of about 3,272,143 (363)
Enantioselective Total Synthesis of (−)‐Blennolide A
AbstractBlennolide A can be synthesized through an enantioselective domino‐Wacker/carbonylation/methoxylation reaction of 7 a with 96 % ee and an enantioselective Wacker oxidation of 7 b with 89 % ee. Further transformations led to the α,β‐unsaturated ester (E)‐17, which was subjected to a highly selective Michael addition, introducing a methyl group ...
Tietze, Lutz Friedjan+4 more
openaire +4 more sources
Aziridination of alkenes is an important route to chiral nitrogen‐containing building blocks. We report that carbamate‐functionalized allylic alcohols undergo highly enantioselective aziridination using achiral dimeric Rh complexes ion‐paired with cinchona alkaloid‐derived chiral cations.
Arthur R. Lit+4 more
wiley +2 more sources
Enantioselective Synthesis of the C(1)-C(6?) Subunit of Zaragozic Acid C
Preparation of the C(1)-C(6?) subunit of Zaragozic acid C is described. The C(5?) methyl-bearing stereocenter is installed by rapid, regioselective opening of a phenylcyclopropyl carbinol with Pearlman?s catalyst (1 atm H2) in 2% triflic acid/methanol.
Carreira Erick M., Ledford Brian E.
doaj
Chiral molecules have similar physicochemical properties, which are different in terms of physiological activities and toxicities, rendering their differentiation and recognition highly significant. Nanozymes, which are nanomaterials with inherent enzyme-
Jing-Jing Dai+4 more
doaj +1 more source
Catalyst screening without catalysis. By combining cyclic voltammetry and DFT calculations we were able to identify a highly active catalyst for the radical arylation of epoxides without performing any reactions. The prevention of chloride binding that leads to catalyst inhibition was established as the key structural feature.
Niklas Schmickler+6 more
wiley +2 more sources
Asymmetric Intramolecular α‐Arylation of Polar Amino Acids Bearing β‐Leaving Groups
Use of enolate chemistry to functionalise amino acids with β‐heteroatom side‐chains (serine, cysteine, threonine, etc.) is hampered by β‐elimination. We show that α‐arylation can be achieved by incorporating the side chain into a saturated heterocycle, making the unwanted elimination a disfavoured 5‐endo‐trig reaction.
Ömer Taspinar+6 more
wiley +2 more sources
Organocatalytic atroposelective construction of axially chiral arylquinones
Axially chiral compounds have widespread use in asymmetric catalysis. Here, the authors disclose a highly enantioselective synthesis of axially chiral o-naphthoquinones by chiral phosphoric acid catalysis and central-to-axial chirality conversion.
Shuai Zhu+8 more
doaj +1 more source
A formal and enantioselective synthesis of (−)-serricornin, the sex pheromone of the cigarette beetle (lasioderma serricorne F.) [PDF]
J. Tércio+3 more
openalex +1 more source
Structural shaping of a highly reactive chiral Mn‐oxo species translates into exceptionally enantioselective C─H oxidation catalyst of cyclohexyl 1,3‐meso diethers (up to >99% ee) leading to polyfunctionalized cyclohexanes. Abstract Chiral polyoxygenated cyclohexanes are valuable constituents of biologically relevant products.
Andrea Palone+7 more
wiley +2 more sources
A carbohydrate approach for the formal total synthesis of (−)-aspergillide C
An enantioselective formal total synthesis of aspergillide C is accomplished using commercially available tri-O-acetyl-D-galactal employing a Ferrier-type C-glycosylation, utilizing a Trost hydrosilylation and protodesilylation as key reactions.
Pabbaraja Srihari+3 more
doaj +1 more source