Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Akash S. Ubale"'
Publikováno v:
The Journal of Organic Chemistry. 87:8104-8117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b034db49ed3b99e04b031dfb50417c1
https://doi.org/10.1021/acs.joc.2c00779
https://doi.org/10.1021/acs.joc.2c00779
Autor:
Moseen A. Shaikh, Pragnya Paramita Samal, Akash S. Ubale, Sailaja Krishnamurty, Boopathy Gnanaprakasam
Publikováno v:
The Journal of organic chemistry. 87(21)
The indium-catalyzed regiospecific coupling of substituted phenol derivatives and quaternary peroxyoxindoles for the synthesis of C2 or C4 benzoxazin-3-one-substituted phenols via skeletal rearrangement is described. This reaction is demonstrated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee5c95360631a860883a26e7d33ec16f
https://pubmed.ncbi.nlm.nih.gov/36269888
https://pubmed.ncbi.nlm.nih.gov/36269888
Publikováno v:
Advanced Synthesis & Catalysis. 363:4876-4882
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::539a685e9eca4f3b9d3fdbf43098d4be
https://doi.org/10.1002/adsc.202100793
https://doi.org/10.1002/adsc.202100793
Publikováno v:
The Journal of Organic Chemistry. 86:9621-9636
For the first time, the sequential reaction of peroxyoxindole that involves base-promoted oxidative fragmentation to isocyanate formation and primary amine or amino alcohol accelerated skeletal rearrangement to synthesize exo-olefinic-substituted qui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2939c4f90edfd0ac27615c105d4af034
https://doi.org/10.1021/acs.joc.1c00889
https://doi.org/10.1021/acs.joc.1c00889
Publikováno v:
The Journal of organic chemistry. 87(12)
Herein, we report alkylative aromatization of tetralone for the synthesis of bioactive naphthols and benzo[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1be0ada7150d82befbfc55abca22ea4c
https://pubmed.ncbi.nlm.nih.gov/35612287
https://pubmed.ncbi.nlm.nih.gov/35612287
Publikováno v:
The Journal of Organic Chemistry. 85:2277-2290
The sp3 C-H alkylation of 9H-fluorene using alcohol and a Ru catalyst via the borrowing hydrogen concept has been described. This reaction was catalyzed by the [Ru(p-cymene)Cl2]2 complex (3 mol %) and exhibited a broad reaction scope with different a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f721fce7388500794a1934ab703a98e
https://doi.org/10.1021/acs.joc.9b02913
https://doi.org/10.1021/acs.joc.9b02913
Publikováno v:
The Journal of organic chemistry. 85(16)
Highly efficient, selective, and direct C-H peroxidation of 9-substituted fluorenes has been achieved using a Mn-2,2'-bipyridine catalyst via radical-radical cross-coupling. Moreover, this method effectively promotes the vicinal bisperoxidation of st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82278e5d3c6d9fa2ec53833726ed15c2
https://pubmed.ncbi.nlm.nih.gov/32678600
https://pubmed.ncbi.nlm.nih.gov/32678600
Publikováno v:
The Journal of organic chemistry. 85(4)
The sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2bcec3e003ff7b49bc4f196552ec1b2c
https://pubmed.ncbi.nlm.nih.gov/31905282
https://pubmed.ncbi.nlm.nih.gov/31905282