Results 31 to 40 of about 56,559 (262)

Pd(II)/tbu-quinolineoxazoline: An Air-stable And Modular Chiral Catalyst System For Enantioselective Oxidative Cascade Cyclization [PDF]

open access: yes, 2009
An air-stable and structurally tunable chiral (t)Bu-quinolineoxazoline/Pd(II) catalyst system has been developed for the enantioselective oxidative cascade cyclization of a variety of disubstituted olefinic substrates, with the apparent advantages of ...
Yang, D, He, W, Zhu, NY, Yip, KT
core   +1 more source

Cyclic Peptoid-Peptide Hybrids as Versatile Molecular Transporters

open access: yesFrontiers in Chemistry, 2021
Addressing intracellular targets is a challenging task that requires potent molecular transporters capable to deliver various cargos. Herein, we report the synthesis of hydrophobic macrocycles composed of both amino acids and peptoid monomers. The cyclic
Claudine Nicole Herlan   +6 more
doaj   +1 more source

Synthesis of Thiomorpholine via a Telescoped Photochemical Thiol-ene/Cyclization Sequence in Continuous Flow [PDF]

open access: yes, 2022
A procedure for the continuous flow generation of thiomorpholine in a two-step telescoped format was developed. The key step was the photochemical thiol-ene reaction of cysteamine hydrochloride and vinyl chloride as low-cost starting materials under ...
Ryan C. , Nelson   +3 more
core   +1 more source

Changing the topology of protein backbone: the effect of backbone cyclization on the structure and dynamics of a SH3 domain

open access: yesFrontiers in Chemistry, 2015
Understanding of the effects of the backbone cyclization on the structure and dynamics of a protein is essential for using protein topology engineering to alter protein stability and function.
Frank H Schumann   +6 more
doaj   +1 more source

Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis

open access: yesChemistryOpen, 2022
Vanadate‐dependent chloroperoxidase from Curvularia inaequalis catalyzes 5‐endo‐trig bromocyclizations of α‐allenols to produce valuable halofunctionalized furans as versatile synthetic building blocks. In contrast to other haloperoxidases, also the more
Janne M. Naapuri   +3 more
doaj   +1 more source

Iron-Promoted Cyclization/Halogenation of Alkynyl Diethyl Acetals [PDF]

open access: yes, 2009
FeCl(3)(-) and FeBr(3)-promoted cyclization/halogenation of alkynyl diethyl acetals has been efficiently realized, selectively affording (E)-2(1-halobenzylidene or alkylidene)-substituted five-membered carbo- and heterocycles which were then efficiently ...
Xu, Tongyu   +3 more
core   +1 more source

Divergent Total Syntheses of Aspidospermidine, N-Methylaspidospermidine, N-Acetylaspidospermidine and Aspido-spermine via a Tandem Cyclization of Tryptamine-Ynamide [PDF]

open access: yes, 2021
The divergent total syntheses of aspidospermidine, N-methylaspidospermidine, N-acetylaspidospermidine and aspidosperm-ine were achieved from a common pentacyclic indoline intermediate.
Maosheng, Cheng   +9 more
core   +1 more source

Nucleophilic and electrophilic cyclization of N-alkyne-substituted pyrrole derivatives: Synthesis of pyrrolopyrazinone, pyrrolotriazinone, and pyrrolooxazinone moieties

open access: yesBeilstein Journal of Organic Chemistry, 2017
Intramolecular nucleophilic and electrophilic cyclization of N-alkyne-substituted pyrrole esters is described. Efficient routes towards the synthesis of pyrrolopyrazinone, pyrrolotriazinone and pyrrolooxazinone have been developed.
Işıl Yenice   +2 more
doaj   +1 more source

The oxime portmanteau motif : released heteroradicals undergo incisive EPR interrogation and deliver diverse heterocycles [PDF]

open access: yes, 2014
OA funded through the RCUK OA block grant.Selective syntheses are now available for compounds of many classes, based on C-centered radicals, exploiting a diverse range of mechanisms.
John C. Walton, Walton, John Christopher
core   +1 more source

Recent Advances in the Biosynthesis of Carbazoles Produced by Actinomycetes

open access: yesBiomolecules, 2020
Structurally diverse carbazole alkaloids are valuable due to their pharmaceutical properties and have been isolated from nature. Experimental knowledge on carbazole biosynthesis is limited. The latest development of in silico analysis of the biosynthetic
Masaya Kobayashi, Tomohisa Kuzuyama
doaj   +1 more source

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