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of 37
pro vyhledávání: '"Brijesh Chandra"'
Publikováno v:
Molecules, Vol 26, Iss 4, p 1025 (2021)
In spite of unique structural, spectroscopic and redox properties, the synthetic variants of the planar, antiaromatic hexaphyrin (1.0.1.0.1.0) derivatives 2, has been limited due to the low yields and difficulty in access to the starting material. A
Externí odkaz:
https://doaj.org/article/d1e84cf0ee5441a0a18780c5ed58a202
Autor:
Brijesh Chandra Tripathi
Publikováno v:
Sociological Bulletin. 72:192-208
This article invites the reader to reflect on the practice and teaching of sociology through reflexivity in India in a new emerging space of liberal arts in private universities. These spaces can be considered as the fringe of sociology teaching. I a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7e16383a3c57e4468e3ee33bf55300d
https://doi.org/10.1177/00380229221151082
https://doi.org/10.1177/00380229221151082
Autor:
Sridatri Nandy, Brijesh Chandra, B. Sathish Kumar, K. V. Jovan Jose, Ishfaq A. Bhat, Rahul Soman, Pradeepta K. Panda, Sk Saddam Hossain
Publikováno v:
The Journal of Organic Chemistry. 86:10280-10287
The first direct fabrication of A2B- and A3-type B(III)subchlorins from meso-ethoxycarbonyl-substituted tripyrrane has been realized by condensation with appropriate acid chlorides (benzoyl chloride, butyryl chloride, and ethyl chlorooxoacetate). The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6e3afda1f58c4bebcb725b11625d99a
https://doi.org/10.1021/acs.joc.1c01001
https://doi.org/10.1021/acs.joc.1c01001
Autor:
Mohammad Khursheed, Hemashri Muguli, Rajan Chellan, Brijesh Chandra Pant, Jogy George, Sendhil Raja Sengodan
Publikováno v:
Optical Engineering. 61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c72d49c66dd2590d0c9576d3b81bde4
https://doi.org/10.1117/1.oe.61.8.086108
https://doi.org/10.1117/1.oe.61.8.086108
Akademický článek
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Autor:
Tripathi, Brijesh Chandra
Publikováno v:
Sociological Bulletin; Apr2023, Vol. 72 Issue 2, p192-208, 17p
Autor:
Young Mee Jung, Chang-Hee Lee, Vincent M. Lynch, Qing He, Srinivas Samala, Brijesh Chandra, Jonathan L. Sessler, Yeonju Park, Ranjan Dutta
Publikováno v:
Chemical Communications. 56:758-761
β,β'-Phenylene bridged hexaphyrin[1.0.1.0.1.0] (naphthorosarin), an expanded porphyrin possessing C3v-symmetry, has been shown to possess unique electronic features. We now report a bimetallic Rh(i)-complex of naphthorosarin retaining 24 π-antiaro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ce41f1d1e3df2483ce786cf2304ba56
https://doi.org/10.1039/c9cc09221h
https://doi.org/10.1039/c9cc09221h
Publikováno v:
The Journal of organic chemistry. 86(15)
Synthesis of tetrapyrrane 8 from acetone and pyrrole via one-step condensation was achieved for the first time along with a much-improved yield of the tripyrrane 9. Diborylation of the tetrapyrrane and subsequent "1 + 1" cyclocoupling with 1,2-diiodo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50705e647e12c7a8f884f23b341a46e0
https://pubmed.ncbi.nlm.nih.gov/34319103
https://pubmed.ncbi.nlm.nih.gov/34319103
Publikováno v:
European Journal of Organic Chemistry. 2017:741-745
Two novel stable β-tetraethylporphycenes (TEPo), namely trans-TEPo (1T) and its unsymmetric isomer cis-TEPo (1C) were synthesized via reductive McMurry coupling of an unsymmetric bipyrrole dialdehyde and isolated through recrystallizations. Both iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf40383bb06c8cfa7a54f18464030106
https://doi.org/10.1002/ejoc.201601584
https://doi.org/10.1002/ejoc.201601584
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 20:429-437
A new subporphyrin namely, hydroxo-5,10,15-tri([Formula: see text]-propyl-3-carbazolyl)subporphyri natoboron(III) 6 has been synthesized via the reported litreture procedure by the condensation of pyridine-tri-[Formula: see text]-pyrrolylborane with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e69077831e12ae43a48757465b66881d
https://doi.org/10.1142/s1088424616500255
https://doi.org/10.1142/s1088424616500255