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Index « Keywords » - entrée « multi‐membered N‐heterocycles »
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multiroute flows < multi‐membered N‐heterocycles < multi‐membered O,N,S‐heterocycles (with at least 2 different heteroatoms)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 34.
[0-20] [0 - 20][0 - 34][20-33][20-40]
Ident.Authors (with country if any)Title
000001 (2008) Melanie Hamon ; Mickael Menand ; Stephane Le Gac ; Michel Luhmer ; Vincent Dalla ; Ivan JabinChemInform Abstract: Calix[6]tris(thio)ureas: Heteroditopic Receptors for the Cooperative Binding of Organic Ion Pairs.
000015 (1998) D. Berkes ; P. Netchitailo ; J. Morel ; B. DecroixChemInform Abstract: Synthesis of Thieno[b]quinolizidines and Hofmann Elimination on Methiodides Derivatives.
000021 (1998) P. Pigeon ; M. Othman ; P. Netchitailo ; B. DecroixChemInform Abstract: Selective Access to N‐Aryl or N‐Alkyl Derivatives of Isoindolo[2,1‐b][2,4]benzo(or thieno)diazepines.
000025 (1998) A. Mamouni ; P. Pigeon ; A. Daich ; B. DecroixChemInform Abstract: Intramolecular Amidoalkylation Cyclizations in Synthesis of Novel Pyrrolo(or Isoindolo)thieno[2]benzazepines.
000032 (2003) Ivan Jabin ; Olivia ReinaudFirst C3υ‐Symmetrical Calix[6](aza)crown.
000043 (1999) Mohamed Othman ; Pascal Pigeon ; Bernard DecroixChemInform Abstract: Synthesis and Reduction of Thieno[2′,3′(3′,2′ or 3′,4′):5,6]azocino[2,1‐a]isoindole‐7,13‐diones.
000045 (2001) Pascal Pigeon ; Mohamed Othman ; Bernard DecroixChemInform Abstract: Thieno[2′,3′:5,6]azepino[2,1‐a]isoindolones from Hydroxylactam‐alcohols via N‐Acyliminium Ion Olefin Cyclization.
000046 (1998) M. Othman ; P. Netchitailo ; B. DecroixChemInform Abstract: Synthesis of Pyrrolidinothieno‐ (or [1]Benzothieno)[3]azepinones from the Corresponding Azepinediones or N‐(Thienyl or [1]Benzothienyl)acetylprolinals.
000051 (1997) M. Othman ; P. Netchitailo ; B. DecroixChemInform Abstract: Intramolecular Cyclization of Amido Acids into Pyrrolidinothieno(or (1) benzothieno)(3)azepinediones.
000052 (1999) Mohamed Othman ; Pascal Pigeon ; Bernard DecroixChemInform Abstract: Polycyclic Systems: Synthesis of Isoindolo[2,1‐b]pyrrolo[1,2‐d][2,4]benzodiazocine and Isoindolo[1,2‐d]pyrrolo[1,2‐a][1,5]benzodiazocine.
000064 (1999) Adam Daich ; Stefan Marchalin ; Pascal Pigeon ; Bernard DecroixChemInform Abstract: Synthesis of Benzo(or Furo)[5,6]azepino[2,1‐a]isoindolone Derivatives: π‐Cyclizations of N‐Acyliminium Ions.
000066 (2009) Abderrahmane Hadou ; Abdulkareem Hamid ; Hilarion Mathouet ; Mohamed-Fadel Deida ; Adam DaichChemInform Abstract: An Easy Access to the Exocyclic Lactams Analogous of the Central Nervous System Active Tricyclic Nitroxapine, Mianserine and Chlothiapine Agents Using N‐Acyliminium Chemistry.
000073 (1998) P. Pigeon ; B. DecroixChemInform Abstract: Novel Approach to Isoindole[2,1‐a]quinolines.
000074 (1993) A. Daich ; B. DecroixChemInform Abstract: Potentially Biological Agents: Synthesis and Reactivity of Thienopyrrolo(1,4)diazepines.
000078 (1997) P. Pigeon ; B. DecroixChemInform Abstract: A New Access to Isoindolo(2,1‐b)(2,4)benzodiazepines Through an N‐ Acyliminium Ion‐Amide Cyclization.
000081 (1999) P. Pigeon ; B. DecroixChemInform Abstract: Diisoindolothieno[2,4]diazepines via a Diastereoselective N‐Acyliminium Ion Cyclization.
000082 (1997) P. Pigeon ; B. DecroixChemInform Abstract: Synthesis of Various Substituted Thieno(2′,3′(or 3′,2′):5,6)azepino(2, 1‐a)isoindol‐6‐ones
000083 (1995) C. Chedru ; B. Decroix ; J. Morel ; F. PovazanecChemInform Abstract: Furo(3,2‐e)pyrrolo(1,2‐a)(1,4)diazepine and Derivatives.
000085 (1997) P. Pigeon ; B. DecroixChemInform Abstract: Tetracyclic Systems: Synthesis of Isoindolo(1,2‐b)thieno(2,3(3,2 or 3, 4)‐e)(1,3)thiazocines and Isoindolo(2,1‐a)thieno(2,3(3,2 or 3,4)‐f)(1, 4) and (1,5)diazocines.
000087 (1996) A. Daich ; P. Ohier ; B. DecroixChemInform Abstract: Synthesis of a New Pyrrolo(1,3)diazepine: 4H‐Pyrrolo(1,2‐a)thieno(2,3‐ e) (1,3)diazepine.
000088 (1997) A. Mamouni ; A. Daich ; B. DecroixChemInform Abstract: Synthesis and Reactivity of Oxopyrrolidinothieno(2)azepinones: Benzazepine Antidepressant Analogues.

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