Results 31 to 40 of about 428 (148)

Diversity-Oriented Synthesis of Dibenzoazocines and Dibenzoazepines via a Microwave-Assisted Intramolecular A3-Coupling Reaction

open access: yes, 2016
An unprecedented, diversity-oriented strategy for the generation of 6,7-dihydro-5H-dibenzo[c,e]azepines and 5,6,7,8-tetrahydrodibenzo[c,e]azocines by a microwave-assisted copper-catalyzed intramolecular A3-coupling reaction is ...
Kristof Van Hecke (1574854)   +7 more
core   +3 more sources

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

open access: yesChemBioChem, Volume 25, Issue 16, August 19, 2024.
Strain‐promoted azide‐alkyne cycloaddition (SPAAC) of site‐selectively cross‐linked human hemoglobin with specifically modified human serum albumin yields a structurally defined protein‐protein conjugate. A circulating solution of the conjugate can provide cooperative oxygen transport and maintain colloid osmotic pressure.
Chi Lee   +2 more
wiley   +1 more source

The first example of 4,7,8,9-tetrahydrothieno-[2,3-d]azocine synthesis by domino reaction of 4-aryl-4,5,6,7-tetrahydrothieno[3,2-c]pyridines with activated alkynes

open access: yes, 2020
1-Aryl-substituted tetrahydrothieno[3,2-c]pyridines easily undergo domino reactions with activated alkynes, giving good yields of the corresponding tetrahydrothieno[2,3-d]azocines.
Chervyakova T.M.   +8 more
core   +2 more sources

Organocalcium Hydride-Catalyzed Intramolecular C(sp3)–H Annulation of Functionalized 2,6-Lutidines

open access: yes, 2023
This work reports an intramolecular C(sp3)–H annulation of functionalized 2,6-lutidines catalyzed by an organocalcium hydride [{(DIPPnacnac)CaH(thf)}2] (DIPPnacnac = CH{(CMe)(2,6-iPr2–C6H3N)}2).
Xin Xu (11989)   +3 more
core   +2 more sources

Synthesis of 6,12-Methanodibenzo[c,f]azocines and 4‑Aryltetrahydroisoquinolines from Aromatic Aldehydes

open access: yes, 2019
A methodology for the synthesis of 7,12-dihydro-5H-6,12-methanodibenzo­[c,f]­azocines from aromatic aldehydes and N-(methoxymethyl)-N-(trimethylsilylmethyl)­benzylamine using catalysis by trifluoroacetic and perchloric acids is described.
Vladimir S. Moshkin (2582062)   +7 more
core   +1 more source

Transformations of tetrahydropyrido[4′,3′:4,5]thieno[2,3-d] pyrimidin-4(3H)-ones in the presence of alkynes bearing electron-withdrawing substituents

open access: yes, 2020
Tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidines in the presence of activated alkynes were transformed into mixtures of pyrimido[5′,4′:4,5]thieno[3,2-d]azocines and spiro[pyridine-4, 5′-thieno[2,3-d]pyrimidines]. © 2012 Springer Science+Business Media
Khrustalev V.N.   +7 more
core   +2 more sources

A photochemical ring expansion of 6- to 8-membered nitrogen heterocycles by [1,3]-sigmatropic rearrangement

open access: yes, 2021
A new route to azocines and benzoazocines from furopyridinones is described through a photochemically induced [1,3]-sigmatropic rearrangement. The method gives access to these 8-membered nitrogen heterocycles from dimethyl squarate in four stages and ...
Sun, Wei   +7 more
core   +1 more source

Transformations of 4,5,6,7-tetrahydrothieno[3,2-c]-and 1,2,3,4- tetrahydrobenzothieno[2,3-c]pyridines in reactions with alkynes activated by electron-withdrawing substituents

open access: yes, 2020
The transformations of tetrahydrothieno[3,2-c]-and tetrahydrobenzothieno[2, 3-c]pyridines in the reactions with acetylenedicarboxylic ester, alkyl propiolates, and acetylacetylene in alcohols were studied.
Sorokina E.A.   +5 more
core   +2 more sources

Interaction, bond formation or reaction between a dimethylamino group and an adjacent alkene or aldehyde group in aromatic systems controlled by remote molecular constraints

open access: yes, 2021
Peri-peri interactions in naphthalene systems control the degree of bond formation between a peri-dimethylamino group and a polarised alkene or aldehyde group.
Bristow, Jonathan C.   +7 more
core   +1 more source

Diversity-oriented synthesis of dibenzoazocines and dibenzoazepines via a microwave-assisted intramolecular A3-coupling reaction

open access: yes, 2010
An unprecedented, diversity-oriented strategy for the generation of 6,7-dihydro-5H-dibenzo[c,e]azepines and 5,6,7,8-tetrahydrodibenzo[c,e]azocines by a microwave-assisted copper-catalyzed intramolecular A(3)-coupling reaction is ...
Van Hecke, Kristof   +15 more
core   +1 more source

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