Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ayyavu, Thirunarayanan"'
Publikováno v:
SynOpen, Vol 03, Iss 04, Pp 157-163 (2019)
Abstract A simple one-pot synthesis of amidopiperazinophanes with a combination of electron-deficient amide groups and electron-rich alkyne and piperazine functionalities has been achieved by using multicomponent reaction (MCR) methodology with the M
Externí odkaz:
https://doaj.org/article/fc23e6f062934d73b1af16edacfb4cc7
Publikováno v:
In Fundamentals and Properties of Multifunctional Nanomaterials 2021:369-404
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 8, Pp o865-o865 (2014)
The title compound, 8,18-dithia-2,6-diaza-13(1,4)-piperidina-1(1,2),4(1,3),7(1,2)-tribenzenaoctadecaphane-10,15-diyne-3,6-dione, C32H30N4O2S2, is composed of a relatively planar bis(2-mercaptophenyl)isophthalamide unit linked to a bridging 1,4-di(but
Externí odkaz:
https://doaj.org/article/d36e7e9ccefe44a0ae8631171501aefc
Autor:
Vijayan Viswanathan, Thothadri Srinivasan, Ayyavu Thirunarayanan, Perumal Rajakumar, Devadasan Velmurugan
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 10, Pp o2921-o2921 (2012)
In the title compound, C16H15IO4S, the dihedral angle between the thiophene and benzene rings is 11.50 (2)°. The methoxy O atoms deviate by 0.0060 (2), −0.1319 (2) and 0.0426 (2) Å from the phenyl ring plane. The crystal packing features C—H...
Externí odkaz:
https://doaj.org/article/f4e55aad63444a47af7e25e5714d0c40
Autor:
Kyunghoon Oh, Kimoon Kim, Ayyavu Thirunarayanan, Ara Lee, Annadka Shrinidhi, Gihyun Sung, Dinesh K. Shetty, Jaehwan Sim, James Brooke Murray
Publikováno v:
Angewandte Chemie International Edition. 56:2395-2398
Chemical proteomics relies primarily on click-chemistry-based protein labeling and biotin-streptavidin enrichment, but these techniques have inherent limitations. Enrichment of intracellular proteins using a totally synthetic host-guest complex is de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73360b6028230580eb8cd5b460d8b9f5
https://doi.org/10.1002/anie.201611894
https://doi.org/10.1002/anie.201611894
Publikováno v:
Journal of Heterocyclic Chemistry. May2016, Vol. 53 Issue 3, p993-996. 4p.
Publikováno v:
Synlett. 25:2127-2132
Several 1:1 and 2:2 oligomeric forms of piperazinophanes with oxa–aza intraannular functionalities and containing various bicyclic ring systems as spacer units were prepared by a one-pot method under simple and mild conditions through a multicompon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39517267ef3302eb796b4d8d9648ede3
https://doi.org/10.1055/s-0034-1378524
https://doi.org/10.1055/s-0034-1378524
Publikováno v:
Proceedings of the National Academy of Sciences, India Section A: Physical Sciences. 84:371-379
One-pot synthesis of novel N-methyl pyrroli- dine dendrimers has been accomplished in good yield via a facile (3?2) cycloaddition of azomethine ylide with chal- cone moiety of the dendrimer as a dipolarophile. All the pyrrolidine dendrimers exhibited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d92beefaf0cf0b86478bfde8f3ceea0
https://doi.org/10.1007/s40010-013-0120-6
https://doi.org/10.1007/s40010-013-0120-6
Publikováno v:
RSC Adv.. 4:41778-41783
S-BINOL based chiral dendrimers with m-terphenyl at the surface and triazole as the bridging unit have been synthesized by a convergent synthetic strategy through the ‘click’ chemistry approach. The resazurin reduction assay method shows that all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f29326e775ba245114260f15db6933c
https://doi.org/10.1039/c4ra04967e
https://doi.org/10.1039/c4ra04967e
Publikováno v:
RSC Adv.. 4:23433-23439
One pot synthesis of crown ether type chiral and achiral 2:2 oligomeric thiadiazolophane 1 and 3 and 3:3 oligomeric thiadiazolophane 2 and 4 with (S)-BINOL and a methylene bis-naphthyl spacer unit has been achieved under simple and mild conditions by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40a1e63a7f3710098e42578072929652
https://doi.org/10.1039/c4ra02672a
https://doi.org/10.1039/c4ra02672a