Results 41 to 50 of about 14,856 (220)

Photo‐Degradable Polyester Networks and Multi‐Photon Printed Objects Based on Cyclic Ketene Acetals

open access: yesAdvanced Functional Materials, EarlyView.
The current work introduces a photoreversible polyester network derived from radical ring‐opening polymerization of cyclic ketene acetals. It combines photoreversible cross‐linking with initiator‐free multi‐photon printing. Reversible network formation, tunable mechanical properties, and selective degradation highlight its potential as a versatile ...
Till Meissner   +5 more
wiley   +1 more source

Methyl (S)-3-((1r*,3R*)-3-((1H-indol-3-yl)methyl)cyclobutane-1-carboxamido)-2-(phenylsulfonamido)propanoate

open access: yesMolbank
The cyclobutane ring has attractive properties as a scaffold in medicinal chemistry but is underused, potentially due to the limited methods available for synthesising highly functionalised cyclobutanes. This short note describes the synthesis of the 1,3-
Helen M. Sheldrake
doaj   +1 more source

Synthetic studies towards d-modified paclitaxel analogues [PDF]

open access: yesJournal of the Serbian Chemical Society, 2012
A synthetic sequence has been developed for the preparation of 9,10-O-diacetyl-4-desmethylene-4β-(3-butenyl)-4α-hydroxy-5-O-mesyltaxicin I-1,2-carbonate 3, an intermediate in the attempted synthesis of cyclobutane paclitaxel analogue.
Matović Radomir   +2 more
doaj   +1 more source

A biorenewable cyclobutane-containing building block synthesized from sorbic acid using photoenergy

open access: yesiScience, 2022
Summary: A novel cyclobutane-containing diacid building block, CBDA-3, was synthesized from sorbic acid using clean, efficient [2 + 2] photocycloaddition.
Micah Mabin   +4 more
doaj   +1 more source

1,3-Bis(4-methylbenzoyl)-2,4-bis(2,4,5-trimethoxyphenyl)cyclobutane

open access: yesIUCrData, 2017
The title compound, C38H40O8, possess an inversion centre at the centroid of the four-membered ring. The dihedral angle between the methylbenzene and trimethoxybenzene rings is 46.19 (8)°.
K. R. Raghavendra   +5 more
doaj   +1 more source

Crystal structures of (E)-5-(4-methylphenyl)-1-(pyridin-2-yl)pent-2-en-4-yn-1-one and [3,4-bis(phenylethynyl)cyclobutane-1,2-diyl]bis(pyridin-2-ylmethanone)

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2020
Recrystallization of (E)-5-phenyl-1-(pyridin-2-yl)pent-2-en-4-yn-1-one at room temperature from ethylene glycol in daylight afforded [3,4-bis(phenylethynyl)cyclobutane-1,2-diyl)bis(pyridin-2-ylmethanone], C32H22N2O2 (3), while (E)-5-(4-methylphenyl)-1 ...
Ivan E. Ushakov   +5 more
doaj   +1 more source

Diversifying molecular and topological space via a supramolecular solid-state synthesis: a purely organic mok net sustained by hydrogen bonds

open access: yesIUCrJ, 2019
A three-dimensional hydrogen-bonded network based on a rare mok topology has been constructed using an organic molecule synthesized in the solid state. The molecule is obtained using a supramolecular protecting-group strategy that is applied to a solid ...
Shalisa M. Oburn   +6 more
doaj   +1 more source

Stereochemical Control in the Matteson Reaction

open access: yesChemistry – A European Journal, EarlyView.
The Matteson homologation is a highly versatile method for the stereoselective insertion of carbenoids into boronic esters. Through iterative application of the process, complex chiral molecules can be synthesized. The stereoselectivity of the reaction is determined by a chiral diol incorporated in the boronic ester.
Hae Mo Lee, Christoph Hirschhäuser
wiley   +1 more source

Synthesis of Novel Triazolo Cyclobutane Nucleoside Analogs [PDF]

open access: yes, 2015
International audienceSynthesis of triazolo-cyclobutane nucleosides analogs is reported. These molecules have been obtained by a short and efficient sequence involving a click azide-alkyne cycloaddition following by cis-hydroxylation in the key step.
N.Thang Ngo   +14 more
core   +1 more source

Cyclopropylamine‐Derived Distonic Iminium Radicals: Photoinduced Strategies in Chemo‐ and Stereo‐Selective Synthesis

open access: yesChemistry – A European Journal, EarlyView.
Cyclopropylamines have emerged as powerful photocatalytic building blocks. Upon light‐induced single‐electron oxidation, they undergo strain‐release ring opening to generate distonic iminium radicals that enable diverse transformations, including ring‐opening functionalization, formal [3 + 2] cycloadditions, radical cascades, and asymmetric bond ...
Maria Chiara Cabua   +3 more
wiley   +1 more source

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