Search results for "diazocine"

showing 10 items of 16 documents

Eight-Membered Rings With Two Heteroatoms 1,2

2022

The chapter titled “Eight-membered Rings with two Heteroatoms 1,2” deals with heterocine rings with two heteroatoms in a 1,2 relationship, namely 1,2-diazocine, 2H-1,2-oxazocine, 2H-1,2-thiazocine, 1,2-dioxocin, 1,2-oxathiocin and 1,2-dithiocin. This article covers the literature from 2007 to 2019 and reports the chemistry of uncondensed derivatives, heterocines fused to carbocycles and heterocycles, as well as bridged heterocines. As usual, in the case that a particular section is not mentioned, it means that no chemistry has been reported. In this article, the “Biosynthesis” paragraph was additionally introduced, since in the latest years the contribution of Nature to the synthesis of dih…

12-DiazocineAntihuman African Trypanosomiasis12-Oxathiocin12-DithiocinAnticancer agentsPhotoisomerizationRing-opening metathesis polymerization2H-12-ThiazocineDiene ring-closing metathesisSettore CHIM/08 - Chimica Farmaceutica12-Dioxocin2H-12-OxazocineAntimalarial agents
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Eight-membered heterocycles with two heteroatoms in a 1,5-relationship of interest in medicinal chemistry

2020

Abstract This review deals with 1,5-diheterocines that exhibited biological properties and covers comprehensively the literature from 2007 to the end of February 2019. Among the six possible heterocyclic systems belonging to the eight-membered rings with two heteroatoms, N, O, and S, five had derivatives showing pharmacological activities: 1,5-diazocines, 1,5-oxazocines, 1,5-thiazocines, 1,5-dioxocins, and 1,5-dithiocins. Instead, literature reported no articles dealing with 1,5-oxathiocins of interest in medicinal chemistry. In addition to uncondensed derivatives, 1,5-diheterocines fused to five- and six-membered carbocycles or heterocycles are covered. Bridged 1,5-diheterocines are covere…

15-Oxazocine15-DithiocinChemistryBiological activityBiological propertyHeteroatom15-Dioxocin15-ThiazocineEight-membered heterocycles with two heteroatoms 15Medicinal chemistryMedicinal chemistry15-Diazocine
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A facile synthesis of 1-ethyl-3-methyl-11-phenyl-1,4-dihydro-5H-pyrazolo[3,4-c][1,5]benzodiazocin-5-ones. A new ring system

2007

The new ring system pyrazolo[3,4-c][1,5]benzodiazocine was obtained through cyclization of the key intermediate of type 6a-d and 9, in refluxing toluene in presence of a catalytic amount of p-toluensulfonic acid, from moderate to high yields

15-benzodiazocinePyrazolo-15-benzodiazocinePyrazoleAntitumor activity
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Eight-Membered Rings With Two Heteroatoms 1,3

2022

Eight-membered rings with two heteroatoms in a 1,3-relationship, namely 1,3-diazocine, 2H-1,3-oxazocine, 2H-1,3-thiazocine, 4H-1,3-dioxocin, 4H-1,3-oxathiocin, and 4H-1,3-dithiocin, are discussed in this chapter, that covers the literature from 2007 to October 2020 (SciFindern search) and reports the chemistry of uncondensed derivatives, heterocines fused to carbocycles and heterocycles, as well as bridged heterocines. Among eight-membered 1,3-diheterocines, 1,3-diazocines and 1,3-oxazocines are the two largest classes, based on the number of publications, mostly due to the studies of the synthesis of these cyclic systems, their pharmacological properties and/or their important industrial a…

Anti-HIV agentsCold-menthol receptor TRPM8 modulators13-DiazocineCholesterylester transfer protein (CETP) inhibitors4H-13-DithiocinSettore CHIM/08 - Chimica FarmaceuticaHistone deacetylase 6 inhibitorsEquilibrative nucleoside transporter 1 (ENT1) inhibitors4H-13-OxathiocinAnticancer agents4H-13-Dioxocin2H-13-OxazocineBiosynthetic pathways of 1 3-heterocines2H-13-Thiazocine
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Eight-membered heterocycles with two heteroatoms in a 1,3-relationship of interest in medicinal chemistry

2022

This chapter deals with 1,3-diheterocines, eight-membered heterocyclic systems with two heteroatoms, N, O and S, in a 1,3 relationship, exhibiting biological properties and exhaustively covers the literature from 2007 to the end of November 2019. The biological results of 1,3-diazocines, 1,3-oxazocines, 1,3-dioxocins and 1,3-thiazocines, that are the largest class of 1,3-diheterocines, were collected together with the few results available for 1,3-oxathiocin and 1,3-dithiocin derivatives at that time.

ChemistryHeteroatomEight-membered heterocycles with two heteroatoms 13 Medicinal chemistry Biological activity 13-Diazocines 13-Oxazocines 13-Thiazocines 13-Dioxocins 13-Oxathiocins 13-DithiocinsSettore CHIM/08 - Chimica FarmaceuticaMedicinal chemistry
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Eight-membered heterocycles with two heteroatoms in a 1,2-relationship of interest in medicinal chemistry

2021

Abstract This chapter treats 1,2-diheterocines, eight membered heterocyclic systems with two heteroatoms, N, O and S, in an 1,2 relationship, exhibiting biological properties and exhaustively covers the literature from 2007 to the end of November 2019. In this period of time 1,2-diazocine, 1,2-oxazocine, 1,2-dioxocin and 1,5-dithiocin ring systems had derivatives exhibiting pharmacological activities. No articles on biological properties have been reported for 1,2-thiazocines and 1,2-oxathiocins. Besides uncondensed derivatives, 1,2-diheterocines fused with five-, six-, and seven-membered carbocycles or heterocycles have been reviewed, as well as bridged 1,2-diheterocines.

Eight-membered heterocycles with two heteroatoms 12 Medicinal chemistry Biological activity 12-Diazocines 12-Oxazocines 12-Dioxocins 12-DithiocinsChemistryBiological propertyHeteroatomOrganic chemistryRing (chemistry)
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Eight-Membered Rings With Two Heteroatoms 1,5

2022

This chapter titled “Eight-membered Rings with two Heteroatoms 1,5” deals eight-membered rings with two heteroatoms in a 1,5-relationship, namely 1,5-diazocine, 1,5-oxazocine, 1,5-thiazocine, 1,5-dioxocin, 1,5-oxathiocin, and 1,5-dithiocin and covers the literature from 2007 to October 2020 (SciFindern search) reporting the chemistry of uncondensed derivatives, diheterocines fused to carbocycles and heterocycles, as well as bridged diheterocines. Among them, the 1,5-diazocine ring system is by far the largest class, based on the number of publications which constituted the 87% of the total amount of the references reported in the range of interest of CHEC IV. Thus, 1,5-diazocines were divid…

Follicle-Stimulant Hormone (FSH) receptor agonists1 5-Dithiocin1 5-OxazocineAnticancer agentsGas permeation membranes1 5-ThiazocinesAntiHCV agentsSmac mimetics1 5-Diazocine1 5-OxathiocinSettore CHIM/08 - Chimica Farmaceutica1 5-DioxocinAntimalarial agents
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CCDC 655687: Experimental Crystal Structure Determination

2008

Related Article: H.V.Ly, H.M.Tuononen, M.Parvez, R.Roesler|2008|Angew.Chem.,Int.Ed.|47|361|doi:10.1002/anie.200703556

Space GroupCrystallographyCrystal System(mu~2~-eta^8^eta^5^-37-Dimethyl-2468-tetraphenyl-2468-tetrabora-15-diazocine)-bis(eta^5^-pentamethyl-cyclopentadienyl)-di-ruthenium hexane solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1546697: Experimental Crystal Structure Determination

2017

Related Article: Adam F. Henwood, Amlan K. Pal, David B. Cordes, Alexandra M. Z. Slawin, Thomas W. Rees, Cristina Momblona, Azin Babaei, Antonio Pertegás, Enrique Ortí, Henk J. Bolink, Etienne Baranoff, Eli Zysman-Colman|2017|J.Mater.Chem.C|5|9638|doi:10.1039/C7TC03110F

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(510-dihydrodiimidazo[12-b:2'1'-d][25]benzodiazocine)-(26-dimethoxy-5-[4-methylpyridin-2-yl]pyrimidin-4-yl)-(26-dimethoxy-5-[4-methylpyridin-2-yl]pyrimidin-3-ium-4-yl)-iridium bis(hexafluorophosphate) acetonitrile diethyl ether solvateExperimental 3D Coordinates
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CCDC 1979408: Experimental Crystal Structure Determination

2021

Related Article: Widukind Moormann, Tobias Tellkamp, Eduard Stadler, Fynn R��hricht, Christian N��ther, Rakesh Puttreddy, Kari Rissanen, Georg Gescheidt, Rainer Herges |2020|Angew.Chem.,Int.Ed.|59|15081|doi:10.1002/anie.202005361

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters12111212a12b-hexahydrodiindeno[71-cd:1'7'-fg][12]diazocineExperimental 3D Coordinates
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