An efficient Ti0.95Cu0.05O1.95 catalyst for ipso – hydroxylation of arylboronic acid and reduction of 4-nitrophenol

2021 ◽  
Vol 133 (3) ◽  
Author(s):  
Shrikanth K Bhat ◽  
Prasanna ◽  
Jagadeesh Prasad Dasappa ◽  
M S Hegde
Keyword(s):  
Author(s):  
Juha Siitonen ◽  
Padmanabha V. Kattamuri ◽  
Muhammed Yousufuddin ◽  
Laszlo Kurti

Unprotected keto- and aldoximes are readily <i>C</i>-allylated with allyl diisopropyl boronate in the presence of arylboronic acid catalysts to yield highly-substituted <i>N</i>-alpha-secondary (2°) and tertiary (3°) hydroxylamines. The method’s synthetic utility is demonstrated with the total synthesis of the trace alkaloid <i>N</i>-methyl-euphococcine. Preliminary experimental and computational mechanistic studies point toward the formation of a boroxine as the active allylating species.<br>


2020 ◽  
Vol 11 (21) ◽  
pp. 5572-5576 ◽  
Author(s):  
Noboru Hayama ◽  
Yusuke Kobayashi ◽  
Eriko Sekimoto ◽  
Anna Miyazaki ◽  
Kiyofumi Inamoto ◽  
...  

An asymmetric thia-Michael addition of arylthiols to α,β-unsaturated carboxylic acids using a thiourea catalyst that bears arylboronic acid and tertiary amine moieties is reported.


2009 ◽  
Vol 11 (6) ◽  
pp. 1441-1443 ◽  
Author(s):  
Masahiro Yoshida ◽  
Yasunobu Shoji ◽  
Kozo Shishido

Tetrahedron ◽  
2014 ◽  
Vol 70 (9) ◽  
pp. 1800-1804 ◽  
Author(s):  
Ru-Ching Lian ◽  
Meng-Hsuan Lin ◽  
Pin-Hsuan Liao ◽  
Jia-Jie Fu ◽  
Meng-Ju Wu ◽  
...  

1993 ◽  
Vol 115 (15) ◽  
pp. 7037-7038 ◽  
Author(s):  
Linda K. Mohler ◽  
Anthony W. Czarnik

2011 ◽  
Vol 372 (1) ◽  
pp. 321-326 ◽  
Author(s):  
Pilli V.V.N. Kishore ◽  
Ananda Kumar Jami ◽  
Viswanathan Baskar
Keyword(s):  

2020 ◽  
Vol 61 (16) ◽  
pp. 151780
Author(s):  
Xing Yi ◽  
Ya-Fang Cao ◽  
Xing Wang ◽  
Hui Xu ◽  
Shu-Rong Ban ◽  
...  

2020 ◽  
Vol 56 (19) ◽  
pp. 2941-2944 ◽  
Author(s):  
Lok Nath Neupane ◽  
Joohee Park ◽  
Pramod Kumar Mehta ◽  
Eun-Taex Oh ◽  
Heon Joo Park ◽  
...  

We present a reaction-based fluorescent probe for Hg2+ and methylmercury based on the displacement reaction of arylboronic acid with mercury species.


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