Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Arunachalam, Kannan"'
Autor:
Winaki P. Sohtun, Arunachalam Kannan, K. Hari Krishna, Dhandayutham Saravanan, Muthuvel Suresh Kumar, Marappan Velusamy
Publikováno v:
Acta Chimica Slovenica, Vol 65, Iss 3, Pp 621-629 (2018)
The title compound bis[2-hydroxybenzylidenehydrazono)(methylthio)methyl]disulfide (1), an S-methyldithiocarbazate derivative with a disulfide bond has been synthesized by the condensation of 2-hydroxybenzaldehyde with S-methyldithiocarbazate. It has
Externí odkaz:
https://doaj.org/article/7640137aee6446df96e6e48ddfdfb4fe
Publikováno v:
IUCrData, Vol 3, Iss 3, p x180461 (2018)
In the title compound, C11H15N3S2, the dithiocarbazate moiety is rotated by 18.73 (8)° with respect to the benzene ring. The dithiocarbazate group adopts an E configuration with respect to the C=N bond of the benzylidene group. Furthermore, in the s
Externí odkaz:
https://doaj.org/article/f56c8d65f3ac4529bb3159089b04f800
Autor:
P Winaki, Sohtun, Arunachalam, Kannan, K Hari, Krishna, Dhandayutham, Saravanan, Suresh Muthuvel, Kumar, Marappan, Velusamy
Publikováno v:
Acta chimica Slovenica. 65(3)
The title compound bis[2-hydroxybenzylidenehydrazono)(methylthio)methyl]disulfide (1), an S-methyldithiocarbazate derivative with a disulfide bond has been synthesized by the condensation of 2-hydroxybenzaldehyde with S-methyldithiocarbazate. It has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71ac450ce6d6c7fc6816f2be06ff3de9
https://pubmed.ncbi.nlm.nih.gov/33562925
https://pubmed.ncbi.nlm.nih.gov/33562925
Autor:
Themmila Khamrang, Arunachalam Kannan, Mohammad Abdulkader Akhbarsha, Dhandayutham Saravanan, Gowdhami Balakrishnan, Winaki P. Sohtun, Mallayan Palaniandavar, Marappan Velusamy
Publikováno v:
Applied Organometallic Chemistry. 34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7715fd47ae5c68804543b869730dffcd
https://doi.org/10.1002/aoc.5593
https://doi.org/10.1002/aoc.5593
Autor:
K. Hari Krishna, Arunachalam Kannan, Muthuvel Suresh Kumar, Dhandayutham Saravanan, Winaki P. Sohtun, Marappan Velusamy
Publikováno v:
Acta Chimica Slovenica, Vol 65, Iss 3, Pp 621-629 (2018)
The title compound bis[2-hydroxybenzylidenehydrazono)(methylthio)methyl]disulfide ( 1 ), an S-methyldithiocarbazate derivative with a disulfide bond has been synthesized by the condensation of 2-hydroxybenzaldehyde with S-methyldithiocarbazate. It ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a1a68d1ccd14c1048a7c74150a1cb08
https://doi.org/10.17344/acsi.2018.4275
https://doi.org/10.17344/acsi.2018.4275
Publikováno v:
Canadian Journal of Chemistry. 95:278-285
In our effort to prepare [m.n]cyclophanes carrying functional groups in their molecular bridges, the thiacyclophanes 14, 19, 20, and 21 have been prepared by simple routes from the pseudo-gem dibromide 10a and the corresponding bis-thiol 10b. The tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::060197e041b80964c2fec054d8f1af59
https://doi.org/10.1139/cjc-2016-0358
https://doi.org/10.1139/cjc-2016-0358
Publikováno v:
IUCrData, Vol 3, Iss 3, p x180461 (2018)
In the title compound, C11H15N3S2, the dithiocarbazate moiety is rotated by 18.73 (8)° with respect to the benzene ring. The dithiocarbazate group adopts anEconfiguration with respect to the C=N bond of the benzylidene group. Furthermore, in the sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be0515834dfd3d6a024006fac4def0b1
https://doi.org/10.1107/s2414314618004613
https://doi.org/10.1107/s2414314618004613
Autor:
Robert W. Buckheit, Mark Cushman, Tracy L. Hartman, Allison A. Johnson, Arunachalam Kannan, Jim A. Turpin, Guozhang Xu, Heather Wargo, Yves Pommier, Karen M. Watson
Publikováno v:
Bioorganic & Medicinal Chemistry. 10:2807-2816
Substituted diarylmethylenepiperidines (DAMPs) were synthesized as conformationally restricted analogues of the alkenyldiarylmethane (ADAM) class of non-nucleoside reverse transcriptase inhibitors (NNRTIs). Although, like the ADAMs, the DAMPs were fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b334f9106ee1719797af4e85d43bbaa
https://doi.org/10.1016/s0968-0896(02)00095-0
https://doi.org/10.1016/s0968-0896(02)00095-0
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 63:o711-o713
In the title compound, C18H16, the [2.2]paracyclophane geometry is restrained to a considerable extent despite the introduction of the extra C=C bridge; typical paracyclophane features, such as the elongated C-C bridges, are still observed. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::987d967bfc8eeaefd3c6d697c80ec524
https://doi.org/10.1107/s0108270107050937
https://doi.org/10.1107/s0108270107050937
Publikováno v:
The Journal of Organic Chemistry. 61:5090-5102
Cyclophanes of the type 1 and 2, with large cavity sizes, have been synthesized from the corresponding dichloride 8 or 8a and o-xylene-�,�?-dithiol (9), p-xylene-�,�?-dithiol (10), or m-terphenyldithiol (11). Similarly, cyclophanes of the typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24e75309ca66445a3902824db4117568
https://doi.org/10.1021/jo950957y
https://doi.org/10.1021/jo950957y