Results 1 to 10 of about 428 (148)

Synthesis of 1-(para-methoxyphenyl)tetrazolyl-Substituted 1,2,3,4-Tetrahydroisoquinolines and Their Transformations Involving Activated Alkynes [PDF]

open access: yesMolecules, 2018
1-(p-Methoxyphenyl)tetrazolyl-substituted 6,7-dimethoxy(6,7-methylenedioxy)-1,2,3,4-tetrahydroisoquinolines formed tetrazolyl-substituted azocines in high yields by using activated alkynes.
Alexander A. Titov   +9 more
doaj   +4 more sources

The First Example of Tetrahydrothieno[3,2-d]Azocines Synthesis

open access: yesTetrahedron, 2008
A novel and efficient one-pot synthesis of thieno[3,2-d]azocines based on tamden transformation of tetrahydropyridine ring was elaborated. © 2008 Elsevier Ltd. All rights reserved.
Svetlana Kovaleva   +2 more
exaly   +6 more sources

Recent Advances in the Synthesis of Hydrogenated Azocine-Containing­ Molecules [PDF]

open access: yesSynthesis (Stuttg), 2017
This review covers recent advances in synthesis of azocine-containing systems. The most approaches towards azocines are discussed. 1 Introduction 2 Ring-Expansion Reaction 2.1 Ring-Expansion Reaction of Cyclopentane Containing the 1,4-Diketone Moiety with Primary Amines (from 5 to 8)
Listratova A, Voskressensky L.
europepmc   +7 more sources

Synthesis of benz[d]azocines (microreview)

open access: yesChemistry of Heterocyclic Compounds, 2016
[Figure not available: see fulltext.][Figure not available: see fulltext.] This review is concerned with two types of efficient methods for the synthesis of benz[d]-azocines: the ring expansion reactions and intramolecular cyclizations.[Figure not available: see fulltext.] © 2016 Springer Science+Business Media New ...
Nevskaya A.A., Voskressensky L.G.
core   +5 more sources

Two Highly Efficient Syntheses of Scalemic Azocines

open access: yesTetrahedron Letters, 1996
Abstract Two approaches to the synthesis of disubstituted azocines in scalemic form, via intramolecular alkylation and olefin metathesis, respectively, are described.
Jeffrey D Winkler, Jeffrey M Axten
exaly   +2 more sources

Synthesis and photophysics of novel biocompatible fluorescent oxocines and azocines in aqueous solution [PDF]

open access: yesPhysical Chemistry Chemical Physics, 2013
The spectroscopic properties in water solution of the different prototropic forms of the strongly fluorescent hemiacetal 4,9-dihydroxy-1,2-dihydro-4,11a-methanooxocino[4,5-b]benzofuran-5(4H)-one (1a, monardine), the aza analogue 4,9-dihydroxy-3,4-dihydro-1H-4,11a-methanobenzofuro[2,3-d]azocin-5(2H)-one (2a, azamonardine) and the respective 2-carboxyl ...
Acuña, A. Ulises   +4 more
openaire   +5 more sources

Synthesis and biological evaluation of some drug-like scaffolds of benzo-and pyrido-fused medium-sized N-heterocycles obtained via intramolecular Friedel-Crafts acylation reactions [PDF]

open access: yesJournal of the Serbian Chemical Society
An unprecedented, concise and environmentally-friendly protocol for the synthesis of benzo-and pyrido-annulated azocinones, azoninones and azecinones 8a–h via Friedel–Crafts reactions is described.
Abd El-Aal Hassan Abdou Kotb
doaj   +1 more source

An access to some functionalized azocine derivatives [PDF]

open access: yesTetrahedron Letters, 2000
The syntheses, from readily accessible 3-alkyl-4-methoxy-1,3,4,5-tetrahydropyridine 1, of functionalized 1,6,7,8-tetrahydroazocine 7 and 1,2,7,8-tetrahydroazocine 9 are reported.
Laurent Gil   +3 more
openaire   +1 more source

Effect of the Azetidine and Azocine Rings of Okaramine B on Insecticidal Activity

open access: yesBioscience, Biotechnology, and Biochemistry, 2000
Four degraded okaramine B (2) products, 4',5'-dihydrookaramine B (3), two azetidine ring-opened compounds (4 and 5) and 1',2',4',5'-tetrahydrookaramine B (6), were prepared and their insecticidal activity was examined. Neither compounds 4 nor 5 showed such activity against silkworms, indicating that the azetidine ring moiety played an important role in
SHIONO, Yoshihito   +2 more
openaire   +2 more sources

Chapter 2 Synthesis of Heteroannulated Azocine Derivatives

open access: yes, 2008
[No abstract available]
Voskressensky L.G.   +3 more
openaire   +3 more sources

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