Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Prakash R. Sultane"'
Publikováno v:
Chemical Communications. 58:6498-6501
A buckybowl formed a tight 2 : 1 supramolecular complex with C60 in the solid-state as well as in solution.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae89c221603216cdd24f65ab14b73842
https://doi.org/10.1039/d2cc01908f
https://doi.org/10.1039/d2cc01908f
Publikováno v:
Journal of Alloys and Compounds. 922:166197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e92dda328b5a4037b1faa96cc35cd96
https://doi.org/10.1016/j.jallcom.2022.166197
https://doi.org/10.1016/j.jallcom.2022.166197
Publikováno v:
Applied Surface Science. 600:154103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f7c1b6f3022354e534c5d8ca4435706
https://doi.org/10.1016/j.apsusc.2022.154103
https://doi.org/10.1016/j.apsusc.2022.154103
Publikováno v:
Angewandte Chemie International Edition. 58:16320-16325
The synthesis and study of a library of cyclic (aryl)(amido)carbenes (CArAmCs), which represent a class of electrophilic NHCs that feature low calculated singlet-triplet gaps (ΔEST =19.9 kcal mol-1 ; B3LYP/def2-TZVP) and exhibit reactivity profiles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0345b33df412101a9da5a099385279e8
https://doi.org/10.1002/anie.201910350
https://doi.org/10.1002/anie.201910350
Autor:
Jungwoo Oh, Christopher W. Bielawski, Yoonseo Jang, Prakash R. Sultane, Dohwan Jung, Eric S. Larsen
Publikováno v:
Applied Surface Science. 572:151405
Beryllium oxide (BeO) is a unique metal oxide that exhibits high thermal conductivity and a high dielectric constant, even though it has a large bandgap energy. These characteristics can potentially address the electromagnetic issues associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15e4b644aa72bc03c01a9103b872ce51
https://doi.org/10.1016/j.apsusc.2021.151405
https://doi.org/10.1016/j.apsusc.2021.151405
Publikováno v:
Polymer International. 67:1664-1669
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02a1ba20702f387d46c173aa1df9c67e
https://doi.org/10.1002/pi.5691
https://doi.org/10.1002/pi.5691
Publikováno v:
Macromolecular rapid communications. 40(19)
Adamantyl vinyl ketone (AVK) and its copolymers are synthesized using reversible addition fragmentation chain-transfer (RAFT) methodology and then degraded using UV light. The polymerization of AVK is found to be controlled as indicated by a linear c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46218d80fd20dd9a18038f4085f618cf
https://pubmed.ncbi.nlm.nih.gov/31334910
https://pubmed.ncbi.nlm.nih.gov/31334910
Publikováno v:
The Journal of Organic Chemistry. 82:1046-1052
The Burgess reagent ([methoxycarbonylsulfamoyl]triethylammonium hydroxide) has historically found utility as a dehydrating agent. Herein we show that, in the presence of dimethyl sulfoxide, the Burgess reagent efficiently and rapidly facilitates the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038b13258593d8783a07f48490dbff85
https://doi.org/10.1021/acs.joc.6b02629
https://doi.org/10.1021/acs.joc.6b02629
Publikováno v:
Tetrahedron Letters. 56:2067-2070
We describe a convenient and practical method for the deprotection of N-benzyloxycarbonyl (Cbz) and benzyl ester groups using NaBH4 and catalytic Pd–C in methanol. Deprotection was very facile and rapid. In situ generation of hydrogen is certainly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b99d1aafd45ced9a6d1d1be9af9144a
https://doi.org/10.1016/j.tetlet.2015.02.131
https://doi.org/10.1016/j.tetlet.2015.02.131
Publikováno v:
The Journal of Organic Chemistry. 77:11349-11354
A very simple and efficient stereoselective approach to cis-2,3-disubstituted piperidines via the reduction of N-acyliminium ion intermediates is described. Application of this methodology is exemplified by the enantioselective total synthesis of (+)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab0e02edc466cdff198fe6619278700a
https://doi.org/10.1021/jo302181k
https://doi.org/10.1021/jo302181k