Zobrazeno 1 - 10
of 23
pro vyhledávání: '"I. N. Chaithanya Kiran"'
Autor:
Rohan Kalyan Rej, Srinivasa Rao Allu, Joyeeta Roy, Ranjan Kumar Acharyya, I. N. Chaithanya Kiran, Yesu Addepalli, V. Dhamodharan
Publikováno v:
Pharmaceuticals, Vol 17, Iss 4, p 494 (2024)
Proteolysis-targeting chimeras (PROTACs) are an emerging therapeutic modality that show promise to open a target space not accessible to conventional small molecules via a degradation-based mechanism. PROTAC degraders, due to their bifunctional natur
Externí odkaz:
https://doaj.org/article/69d9aed60c0f4b92ab64c630ddd926f2
Publikováno v:
Organic Letters. 25:3623-3627
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc4827458a84edd798105828b2ebeaf2
https://doi.org/10.1021/acs.orglett.3c00943
https://doi.org/10.1021/acs.orglett.3c00943
Publikováno v:
ChemCatChem. 12:5613-5617
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dba18e030d3064a71b5842a93f9dee6a
https://doi.org/10.1002/cctc.202001202
https://doi.org/10.1002/cctc.202001202
Autor:
Thien Phuc Le, Kyosuke Morimoto, Masato Kitamura, Sudipta Kumar Manna, I. N. Chaithanya Kiran, Shinji Tanaka
Publikováno v:
Chemistry – An Asian Journal. 14:3283-3290
A ZnII complex of a C2 -chiral bisamidine-type sp2 N bidentate ligand (LR ) possessing two dioxolane rings at both ends catalyzes a highly efficient quinone asymmetric Diels-Alder reaction (qADA) between o-alkoxy-p-benzoquinones and 1-alkoxy-1,3-buta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d902640d2276093ffead301a166b8c1a
https://doi.org/10.1002/asia.201900995
https://doi.org/10.1002/asia.201900995
Autor:
Huacheng Xu, Chandraiah Lagishetti, Zhen Wang, R. Santhosh Reddy, I. N. Chaithanya Kiran, Yun He
Publikováno v:
The Journal of Organic Chemistry. 82:1823-1832
Transition-metal-free inverse electron-demand aza Diels-Alder and domino [4+2]/[2+2] cycloaddition reaction of arynes and N-sulfonyl ketimines has been demonstrated. This novel, mild, and efficient protocol allows rapid access to isothiazole dioxide-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36e85678af3a24d39e92a02110838832
https://doi.org/10.1021/acs.joc.6b02667
https://doi.org/10.1021/acs.joc.6b02667
Autor:
Kyosuke, Morimoto, Thien Phuc, Le, Sudipta Kumar, Manna, I N Chaithanya, Kiran, Shinji, Tanaka, Masato, Kitamura
Publikováno v:
Chemistry, an Asian journal. 14(19)
A Zn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ff6222fe38174232a6f8786a812ad453
https://pubmed.ncbi.nlm.nih.gov/31456303
https://pubmed.ncbi.nlm.nih.gov/31456303
Publikováno v:
Tetrahedron Letters. 57:3481-3484
Bioactive indolo[3,2- j ]phenanthridine alkaloids, calothrixin A, B, and their analogues have been synthesized via formal cycloaddition of arynes and 2-aminophenanthridinedione as the key step, which proceeds through successive C–C/C–N bond forma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcbca4b947ba26dbfe3274983b7c5c88
https://doi.org/10.1016/j.tetlet.2016.06.091
https://doi.org/10.1016/j.tetlet.2016.06.091
Publikováno v:
Organic Letters. 18:3818-3821
A novel "one-pot" aryne transformation is described that affords various 4-quinolone derivatives without recourse to transition-metal catalysis. Arynes react with aza-Morita-Baylis-Hillman (AMBH) adducts through a cascade sequence involving an insert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e417fb1e9937c9831fdc89cccf680b2
https://doi.org/10.1021/acs.orglett.6b01830
https://doi.org/10.1021/acs.orglett.6b01830
Autor:
Piyush K. Agarwal, Kyriacos C. Nicolaou, Xinghua Zhou, Yu Lan, Bei Cao, Lei Zhu, Biao Xu, Huacheng Xu, Yun He, Ruocheng Yu, I. N. Chaithanya Kiran, Cheng Zou
Publikováno v:
Chemistry - A European Journal. 22:7696-7701
A mild and practical method for the construction of heterocycles from N-substituted 2-oxazolones through cascade, BF3 ⋅Et2 O/H2 O-catalyzed reactions involving iminium ion generation and trapping by external or internal olefinic and aryl moieties i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81b91625ebaa50172f6e2679e06bfb27
https://doi.org/10.1002/chem.201601471
https://doi.org/10.1002/chem.201601471
Publikováno v:
ChemCatChem. 12:5569-5569
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d46edad4b8c9fe70d29fda037e9d97d
https://doi.org/10.1002/cctc.202001647
https://doi.org/10.1002/cctc.202001647