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Published in 2019 at "European Journal of Organic Chemistry"
DOI: 10.1002/ejoc.201900463
Abstract: An operationally simple method has been developed for the preparation of N‐unsubstituted benzotriazoles by diazotization and intramolecular cyclization of a wide range of 1,2‐aryldiamines under mild conditions, using a polymer‐supported nitrite reagent and p‐tosic acid.… read more here.
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Published in 2019 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/s10593-019-02608-0
Abstract: Synthetic approach toward pyridone-substituted furan-2(5H)-ones has been described. Intramolecular cyclization of these compounds leads to novel 7-substituted furo[3,4-f]isoquinolines in moderate to high yields. read more here.
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Published in 2017 at "Chemical Engineering Science"
DOI: 10.1016/j.ces.2017.07.034
Abstract: Abstract Multi-cyclic hydrocarbons from biomass are sustainable alternative for jet fuel. Here we report an unexpected hydrogenated intramolecular cyclization of diphenylmethane derivatives synthesized by alkylation of bio-derived compounds. With the presence of commonly used zeolite-Pd/C… read more here.
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Published in 2019 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2018.12.008
Abstract: Abstract π-Extended oxepins 1 and dimer 8 were synthesized by the benzannulation of the corresponding asymmetric diarylacetylene derivatives and 2-(phenylethynyl)benzaldehyde followed by the Cu-catalyzed intramolecular cyclization. The optical properties of the π-extended oxepins 1 and… read more here.
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c01672
Abstract: A synthesis to access rarely described 3-amino-5-fluoroalkylfurans has been developed by cyclization of easily accessible fluorovinamides. This method is rapid and simple and affords the desired furans as hydrochloride salts in quantitative or nearly quantitative… read more here.
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00539
Abstract: Herein, we report a new method of synthesizing of 2-aminobenzofuran 3-enes via the formal C-S insertion reaction of alkyne-tethered diazo compounds. Metal carbene, as a kind of active synthetic intermediate, plays a very important role… read more here.
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Published in 2020 at "ACS Omega"
DOI: 10.1021/acsomega.9b04384
Abstract: Glutamine (Gln) residues located at N-termini undergo spontaneous intramolecular cyclization, causing the formation of pyroglutamic acid (pGlu) residues. pGlu residues have been detected at the N-termini in various peptides and proteins. The formation of pGlu… read more here.
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Published in 2018 at "Organic chemistry frontiers"
DOI: 10.1039/c8qo00444g
Abstract: Consecutive intermolecular/intramolecular cyclization between N-arylglycine derivatives and 2-hydroxylstyrenes was realized through radical cation salt-initiated sp3 C–H bond oxidation. This reaction provided a new route to forge this biologically important polycyclic benzofuroquinoline skeleton in a single… read more here.
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Published in 2022 at "Chemical communications"
DOI: 10.1039/d2cc06026d
Abstract: We developed an intramolecular cyclization of m-homoprenylphenols and related m-prenylphenols to bicyclic skeletons by hypervalent iodine reagents through an oxidative nucleophilic aromatic substitution using the prenyl group as a carbon nucleophile. The reaction was applicable… read more here.
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Published in 2022 at "RSC Advances"
DOI: 10.1039/d2ra06097c
Abstract: A highly efficient method for the facile access of isoquinolines and isoquinoline N-oxides via a Cu(i)-catalyzed intramolecular cyclization of (E)-2-alkynylaryl oxime derivatives in water has been developed. This protocol was performed under simple and mild… read more here.
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Published in 2017 at "Synthetic Communications"
DOI: 10.1080/00397911.2016.1263892
Abstract: ABSTRACT Simple and efficient one-pot synthesis of 5-substituted isoxazoles and pyrazoles has been developed. The formation of the target isoxazoles and pyrazoles is initiated by 1,2-nucleophilic addition of generated in situ hydroxylamine or hydrazine to… read more here.