Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Michal Rachel Suissa"'
Publikováno v:
European Journal of Organic Chemistry. 2008:2887-2894
The overcrowded bistricyclic aromatic enes (BAEs) [10-[10-(dicyanomethylene)-9(10H)-anthracenylidene]-9(10H)-anthracenylidene]propanedinitrile (7) and [10-[10-oxo-9(10H)-anthracenylidene]-9(10H)-anthracenylidene)]propanedinitrile(8) were synthesized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b5507b921173c4251e79d82491d5c73
https://doi.org/10.1002/ejoc.200701125
https://doi.org/10.1002/ejoc.200701125
Publikováno v:
RSC Advances
RSC Advances, Royal Society of Chemistry, 2014, 4, pp.24729-24735. ⟨10.1039/C4RA02992E⟩
RSC Advances, Royal Society of Chemistry, 2014, 4, pp.24729-24735. ⟨10.1039/C4RA02992E⟩
International audience; The structural and conformational properties of morphine and protonated morphine (morphinum) in the gas phase and in water solution have been explored with quantum calculations. Fully optimized calculations using the cc-pVTZ b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fef050fb57a7c2746e35d4743051f22
https://hal.archives-ouvertes.fr/hal-01024315/document
https://hal.archives-ouvertes.fr/hal-01024315/document
Autor:
Amalia Levy, Yitzhak Tapuhi, Shmuel Cohen, Paul Ulrich Biedermann, Michal Rachel Suissa, Israel Agranat
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :93-100
The objective of the research was to study the e ff ects of alkylidene bridges on the conformations and the conformational behaviour of overcrowded homomerous bistricyclic aromatic ethenes ( 1 ). The isopropylidene- bridged bistricyclic ethene 2 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03458af49ace8e7a029555c82d77b3b8
https://doi.org/10.1039/a906696i
https://doi.org/10.1039/a906696i
Autor:
Michal Rachel Suissa, Israel Agranat
Publikováno v:
Structural Chemistry. 4:59-66
syn-5,5′-Bis-5H-dibenzo[a,d]cyclohepten-5-ylidene (2syn), an overcrowded bistricyclic aromatic ene with central seven-membered rings, undergoes a thermal isomerization to the anti stereoisomer (2anti) at elevated temperatures, with ΔG inv ≯ (174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::048cc8ffd9797da4b49827481361cece
https://doi.org/10.1007/bf00672100
https://doi.org/10.1007/bf00672100
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2962596bdfae793667f57978524069ee
https://doi.org/10.1002/chin.199104187
https://doi.org/10.1002/chin.199104187
Autor:
Michal Rachel Suissa, Israel Agranat
Publikováno v:
ChemInform. 24
syn-5,5′-Bis-5H-dibenzo[a,d]cyclohepten-5-ylidene (2syn), an overcrowded bistricyclic aromatic ene with central seven-membered rings, undergoes a thermal isomerization to the anti stereoisomer (2anti) at elevated temperatures, with ΔG inv ≯ (174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f7ba691a657ccedd1e1150d1ac51e5c
https://doi.org/10.1002/chin.199337113
https://doi.org/10.1002/chin.199337113
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2b5ccdb224d79974cec2633115e073c
https://doi.org/10.1002/chin.199336049
https://doi.org/10.1002/chin.199336049
Autor:
Michal Rachel Suissa, Israel Agranat
Publikováno v:
ChemInform. 25
A topographical approach to the synthesis of large PAHs of the peropyrene series by the Clar reaction, the reductive coupling of 1-phenalenone type aromatic ketones, is outlined. Attention is drawn to the active peri positions of the PAKs radical ani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e189cf0e4d9f7edeaaef909052d91441
https://doi.org/10.1002/chin.199430272
https://doi.org/10.1002/chin.199430272
Autor:
P. Ulrich Biedermann, Israel Agranat, Shmuel Cohen, Amalia Levy, Michal Rachel Suissa, Yitzhak Tapuhi
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34d7142ebee11e7fb55261a2f9892b63
https://doi.org/10.1002/chin.200015021
https://doi.org/10.1002/chin.200015021
Autor:
Israel Agranat, Michal Rachel Suissa
Publikováno v:
Polycyclic Aromatic Compounds. 3:51-61
A topographical approach to the synthesis of large PAHs of the peropyrene series by the Clar reaction, the reductive coupling of 1-phenalenone type aromatic ketones, is outlined. Attention is drawn to the active peri positions of the PAKs radical ani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c58122961bfe6797e729e0b692111cf8
https://doi.org/10.1080/10406639208048326
https://doi.org/10.1080/10406639208048326