Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Keshaba N. Parida"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 992-997 (2018)
Due to their closely matched reactivity, the coupling of two dissimilar ketone enolates to form a 1,4-diketone remains a challenge in organic synthesis. We herein report that umpolung of a ketone trimethylsilyl enol ether (1 equiv) to form a discrete
Externí odkaz:
https://doaj.org/article/c3e6dbce9ef34523917afb50f45c6973
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ad59bca9b3d7ff0ea2579cb15a81987
https://doi.org/10.1002/chem.202203997
https://doi.org/10.1002/chem.202203997
Autor:
Nathan D. Bamberger, Dylan Dyer, Keshaba N. Parida, Tarek H. El-Assaad, Dawson Pursell, Dominic V. McGrath, Manuel Smeu, Oliver L. A. Monti
Publikováno v:
The Journal of Physical Chemistry C. 126:6653-6661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48c74f308285aeaa81acd2fc9aa20f7d
https://doi.org/10.1021/acs.jpcc.2c00761
https://doi.org/10.1021/acs.jpcc.2c00761
Autor:
Tarek H. El-Assaad, Jayden Zhu, Anjitha Sebastian, Dominic V. McGrath, Ishita Neogi, Keshaba N. Parida
Publikováno v:
Organic Chemistry Frontiers. 9:5675-5725
Dioxiranes are extremely useful multitasking agents for a broad spectrum of chemical transformations. This review collates the history of dioxiranes over the last fifty years in the realm of organic and materials chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b81cf0e00288ff5cd333a7ceb920df31
https://doi.org/10.1039/d2qo01005d
https://doi.org/10.1039/d2qo01005d
Publikováno v:
Journal of Materials Chemistry C. 10:16949-16982
Spacer manoeuvring by fluorination to achieve ambient stability in perovskites towards oxygen, moisture, and light.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::debf408fc46aaad8da1ddb1c5f01e333
https://doi.org/10.1039/d2tc03985k
https://doi.org/10.1039/d2tc03985k
Thiosulfonates are accessed by oxidation of feed-stock thiols using either DMP in DCM or IBX in MeCN at rt (~30 degree C). The protocol gives access to a variety of thiosulfonates in good to excellent yields from both aromatic and aliphatic thiols. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89bc46a7c7d1325b94838e23115f3330
https://doi.org/10.26434/chemrxiv-2023-q24pc
https://doi.org/10.26434/chemrxiv-2023-q24pc
