Results 1 to 10 of about 46,609 (242)

Highly Diastereoselective Synthesis of Spiropyrazolones [PDF]

open access: yesMolecules, 2015
We report a highly diastereoselective synthesis of spiropyrazolones catalyzed by secondary amines. The reported Michael-Aldol cascade reaction affords the desired spiropyrazolones bearing four chiral centers as a single diastereomer in excellent yields.
Victor Ceban   +3 more
doaj   +6 more sources

Enantio-, atrop-, and diastereoselective macrolactonization to access type III cyclophanes [PDF]

open access: yesNature Communications
Although chiral substituents have been incorporated into ansa chains to stabilize the conformations of cyclophanes and modulate the biological activities of pharmaceuticals, the asymmetric syntheses of these atropisomers relies on substrate-induced ...
Jiaming Wang   +4 more
doaj   +2 more sources

Diastereoselective Hydrogenation in the Preparation of Fine Chemicals [PDF]

open access: yesTopics in Catalysis, 2018
Heterogeneous catalytic diastereoselective hydrogenation is reviewed with a special emphasis on its application in the preparation of fine ...
Kukula, Pavel, Prins, Roel
core   +6 more sources

Asymmetric Synthesis of Tetrasubstituted α-Aminophosphonic Acid Derivatives

open access: yesMolecules, 2021
Due to their structural similarity with natural α-amino acids, α-aminophosphonic acid derivatives are known biologically active molecules. In view of the relevance of tetrasubstituted carbons in nature and medicine and the strong dependence of the ...
Aitor Maestro   +5 more
doaj   +1 more source

Nucleotide Analogues Bearing a C2′ or C3′-Stereogenic All-Carbon Quaternary Center as SARS-CoV-2 RdRp Inhibitors

open access: yesMolecules, 2022
The design of novel nucleoside triphosphate (NTP) analogues bearing an all-carbon quaternary center at C2′ or C3′ is described. The construction of this all-carbon stereogenic center involves the use of an intramoleculer photoredox-catalyzed reaction ...
Amarender Manchoju   +8 more
doaj   +1 more source

Phytophenol Dimerization Reaction: From Basic Rules to Diastereoselectivity and Beyond

open access: yesMolecules, 2022
Phytophenol dimerization, which is a radical-mediated coupling reaction, plays a critical role in many fields, including lignin biosynthesis. To understand the reaction, 2,2-diphenyl-1-picrylhydrazyl radical was used to initiate a series of phytophenol ...
Shuqin Liu   +5 more
doaj   +1 more source

Diastereoselective Formation of trans-HC(O)SH Through Hydrogenation of OCS on Interstellar Dust Grains [PDF]

open access: yes, 2021
With the presence of evermore complex S-bearing molecules being detected lately, studies on their chemical formation routes need to keep up the pace to rationalize observations, suggest new candidates for detection, and provide input for chemical evolution models.
arxiv   +1 more source

Methods for the synthesis of polyhydroxylated piperidines by diastereoselective dihydroxylation: Exploitation in the two-directional synthesis of aza-C-linked disaccharide derivatives [PDF]

open access: yes, 2005
Background: Many polyhydroxylated piperidines are inhibitors of the oligosaccharide processing enzymes, glycosidases and glycosyltransferases. Aza-C-linked disaccharide mimetics are compounds in which saturated polyhydroxylated nitrogen and oxygen ...
Adam Nelson   +8 more
core   +3 more sources

Diastereoselective Synthesis of Benzoxanthenones

open access: yesChemistry – An Asian Journal, 2020
AbstractAn oxidative catalytic vanadium(V) system was developed to access the naturally nonabundant diastereomers of carpanone from the corresponding alkenyl phenol monomer in one pot by tandem oxidation, oxidative coupling, and 4+2 cyclization. This system was applied to the synthesis of two other analogues of carpanone.
William C. Neuhaus, Marisa C Kozlowski
openaire   +4 more sources

Syntheses of (+)-30-epi-, (-)-6-epi-, (±)-6,30-epi-13,14-didehydroxyisogarcinol and (±)-6,30-epi-garcimultiflorone A utilizing highly diastereoselective, Lewis acid-controlled cyclizations [PDF]

open access: yes, 2016
The first syntheses of 13,14-didehydroxyisogarcinol (6) and garcimultiflorone A (5) stereoisomers are reported in six steps from a commercially available phloroglucinol.
Boyce, Jonathan H.   +2 more
core   +1 more source

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