Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Sundararaman Venkatraman"'
Autor:
Rajneesh Misra, Sundararaman Venkatraman, Viswanathan Baskar, Viswanathan Prabhuraja, Tavarekere K. Chandrashekar
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 180:845-872
Various supramolecular assemblies based on expanded porphyrins building blocks containing sulfur and/or selenium in the core, formed through multiple non-covalent hydrogen bonding interactions are highlighted. Specifically, modified expanded porphyri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c8bf9baccd97e70d374cf09559c7cbd
https://doi.org/10.1080/10426500590906364
https://doi.org/10.1080/10426500590906364
Autor:
Tavarekere K. Chandrashekar, Mathias O. Senge, Ritesh Kumar, C. Vijayan, Alexandra Kelling, Sundararaman Venkatraman, Kaladevi Sendhil, Jeyaraman Sankar
Publikováno v:
Chemistry - A European Journal. 10:1423-1432
Ferrocenyl macrocyclic conjugates involving 22 pi oxasmaragdyrins and 18 pi oxacorroles have been synthesized and characterized. The direct covalent linkage of the ferrocenyl moiety to the meso position of the macrocycle is achieved by simple oxidati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c34a7eff80e6e9965fa8374bc9389e7
https://doi.org/10.1002/chem.200305558
https://doi.org/10.1002/chem.200305558
Autor:
Venkataramanarao G. Anand, Tavarekere K. Chandrashekar, Simi K. Pushpan, Sundararaman Venkatraman
Publikováno v:
Journal of Chemical Sciences. 115:711-720
Expanded porphyrins containing seven pyrrole/heterocyclic rings linked in a cyclic fashion are termed heptaphyrins. The number ofπ-electrons in heptaphyrins depends on the number ofmeso carbon bridges used to link the heterocyclic rings, accordingly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e18decd583ef5d746c2b87fab737ce5b
https://doi.org/10.1007/bf02708261
https://doi.org/10.1007/bf02708261
Autor:
Simi K. Pushpan, Sundararaman Venkatraman, Tavarekere K. Chandrashekar, Jeyaraman Sankar, Harapriya Rath, Venkataramanarao G. Anand
Publikováno v:
Journal of Chemical Sciences. 114:311-338
Porphyrins and metallopophyrins have attracted the attention of chemists for the past 100 years or more owing to their widespread involvement in biology. More recently, synthetic porphyrins and porphyrin-like macrocycles have attracted the attention
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db73cadae879a952a1f3ebd073f4187c
https://doi.org/10.1007/bf02703823
https://doi.org/10.1007/bf02703823
Autor:
Venkataramanarao G. Anand, Sundararaman Venkatraman, Tavarekere K. Chandrashekar, Seenichamy Jeyaprakash Narayanan
Publikováno v:
Journal of Porphyrins and Phthalocyanines. :403-409
Syntheses, characterization and spectroscopic studies of meso-mesityl substituted rubyrins are reported. Specifically, it has been shown that these rubyrins behave differently from the meso-phenyl containing rubyrins in their structure. 1 H NMR studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea1b2273094862e98fd4c08570f2d725
https://doi.org/10.1142/s1088424602000506
https://doi.org/10.1142/s1088424602000506
Autor:
Alagar Srinivasan, A. K. Gupta, Venkataramanarao G. Anand, Tavarekere K. Chandrashekar, K Pushpan Simi, Sundararaman Venkatraman
Publikováno v:
Tetrahedron Letters. 42:3391-3394
The synthesis and characterization of new aromatic 26π macrocycles obtained from the acid catalyzed 4+3 coupling reaction of core modified tripyrrane and tetrapyrrane are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36f0738d19218f983ac7db287821a339
https://doi.org/10.1016/s0040-4039(01)00451-8
https://doi.org/10.1016/s0040-4039(01)00451-8
Core-Modified Hexaphyrins; Characterization of Two- and Four-Ring Inverted 26 π Aromatic Macrocycles
Autor:
Uwe Schilde, Sundararaman Venkatraman, Bhawani S. Joshi, Mathias O. Senge, C. L. Khetrapal, Harapriya Rath, Venkataramanarao G. Anand, Jeyaraman Sankar, Tavarekere K. Chandrashekar
Publikováno v:
Organic Letters. 5:3531-3533
[reaction: see text] Synthesis and structural characterization of aromatic core-modified 26 pi hexaphyrin analogues are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::990a712807a90615c9023e0225273b97
https://doi.org/10.1021/ol035408q
https://doi.org/10.1021/ol035408q
Autor:
Venkataramanarao G. Anand, Simi K. Pushpan, Tavarekere K. Chandrashekar, Sundararaman Venkatraman, Jeyaraman Sankar
Publikováno v:
ChemInform. 33
Successful syntheses of two new aromatic core modified oxybenziporphyrins by a simple '3 + 1' methodology and the first aromatic core modified oxybenziporphyrin palladium complex are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ec9c0bb1b55e612e2d1fb98a0a47ed2
https://doi.org/10.1002/chin.200227152
https://doi.org/10.1002/chin.200227152
Autor:
Sundararaman Venkatraman, Tavarekere K. Chandrashekar, Bashyam Sridevi, Suhash R. Dey, Seenichamy Jeyaprakash Narayanan, Venkataramanarao G. Anand
Publikováno v:
Synlett. 2000:1834-1836
Synthesis of porphyrins containing one to four ferrocenyl groups on the meso carbons is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c6cdef9e39e1d152b1154ad24b48078
https://doi.org/10.1055/s-2000-8700
https://doi.org/10.1055/s-2000-8700
Publikováno v:
Angewandte Chemie (International ed. in English). 46(13)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c1476dbf93d371dfbd8f5a9c87c663f
https://pubmed.ncbi.nlm.nih.gov/17309088
https://pubmed.ncbi.nlm.nih.gov/17309088