Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Saeesh R. Mangaonkar"'
Autor:
Saeesh R. Mangaonkar, Hiroki Hayashi, Wataru Kanna, Suvankar Debbarma, Yu Harabuchi, Satoshi Maeda, Tsuyoshi Mita
Publikováno v:
Precision Chemistry, Vol 2, Iss 3, Pp 88-95 (2024)
Externí odkaz:
https://doaj.org/article/cd72da34cc844f3280f92675615f1694
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1778-1805 (2018)
Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Variou
Externí odkaz:
https://doaj.org/article/83c714e3d7d84ae883402fc88016ceea
Autor:
Saeesh R. Mangaonkar, Hiroki Hayashi, Hideaki Takano, Wataru Kanna, Satoshi Maeda, Tsuyoshi Mita
Publikováno v:
ACS Catalysis. 13:2482-2488
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29b07c1b35f63571462e1e9fa22a23ac
https://doi.org/10.1021/acscatal.2c06192
https://doi.org/10.1021/acscatal.2c06192
Publikováno v:
ChemistrySelect. 5:10754-10758
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::394f4a765d642b7d4d0fd50401e78314
https://doi.org/10.1002/slct.202002860
https://doi.org/10.1002/slct.202002860
Autor:
Saeesh R. Mangaonkar, Fateh V. Singh
Publikováno v:
Synthesis. 51:4473-4486
A convenient approach for the synthesis of β-cyanoepoxides is illustrated by iodine(III)-catalyzed epoxidation of electron-deficient β-cyanostyrenes, wherein the active catalytic iodine(III) species was generated in situ. The epoxidation of β-cyan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66441e6816aa9a5b470fa257adeb8b01
https://doi.org/10.1055/s-0039-1690621
https://doi.org/10.1055/s-0039-1690621
Autor:
Fateh V. Singh, Saeesh R. Mangaonkar
Publikováno v:
Synthesis. 50:4940-4948
An alternative route for the synthesis of 2-arylbenzofurans is described by iodine(III)-catalyzed oxidative cyclization of 2-hydroxystilbenes using 10 mol% (diacetoxyiodo)benzene [PhI(OAc)2] as catalyst in the presence of m-chloroperbenzoic acid. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57831045829b0cde7f87a844677ab217
https://doi.org/10.1055/s-0037-1610650
https://doi.org/10.1055/s-0037-1610650
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1778-1805 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1778-1805 (2018)
Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0384ee10f2e69526061cc591decd1a3
https://doi.org/10.3762/bjoc.14.152
https://doi.org/10.3762/bjoc.14.152
Publikováno v:
Synthetic Communications. 48:2169-2176
An elegant approach for the rapid synthesis of β-cyanoepoxides 3 by the epoxidation of β-cyanostyrenes 1 with PIDA 2a is described. The epoxidation of β-cyanostyrenes 1 was performed with 1.2 equiv. of PIDA 2a in MeCN-H2O (1:1) at room temperature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92048346e4ecce66a3738c1014247af9
https://doi.org/10.1080/00397911.2018.1479760
https://doi.org/10.1080/00397911.2018.1479760
Publikováno v:
Synlett. 29:199-202
An alternative approach is described for the oxidation of organosulfides to the corresponding organosulfones by using trifluoromethyl 3-oxo-1λ3,2-benziodoxole-1(3H)-carboxylate as an oxidant. The oxidation of the sulfides was performed by using 2.4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da554a58ded0963b5b2614f500695f92
https://doi.org/10.1055/s-0036-1588575
https://doi.org/10.1055/s-0036-1588575