scholarly journals Modified Conditions for Copper-catalyzed ipso-Thiolation of Arylboronic Acid Esters with Thiosulfonates

2018 ◽  
Vol 47 (1) ◽  
pp. 85-88 ◽  
Author(s):  
Kazuya Kanemoto ◽  
Suguru Yoshida ◽  
Takamitsu Hosoya
Keyword(s):  
1971 ◽  
Vol 49 (10) ◽  
pp. 1766-1770 ◽  
Author(s):  
R. J. Bose ◽  
M. D. Peters

The mass spectra of a number of phenylboronic acid esters of 1,2- and 1,3-diols are examined and the presence and origin of the tropylium rearrangement ion is established.


2021 ◽  
Author(s):  
Yu Tokita ◽  
Masaru Katoh ◽  
Kentaro Kosaka ◽  
Yoshihiro Ohta ◽  
Tsutomu Yokozawa

Suzuki-Miyaura catalyst-transfer condensation polymerization (CTCP) of fluorene-thiophene biaryl monomers was investigated for the synthesis of well-defined poly(fluorene-alt-thiophene). Model reactions of α,ω-dibromo(fluorene-thiophene) with arylboronic acid esters showed that t-Bu3P Pd and...


Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 1832-P
Author(s):  
ANNA SANTORO ◽  
PENG ZHOU ◽  
YAN ZHU ◽  
ODILE D. PERONI ◽  
ANDREW T. NELSON ◽  
...  

2019 ◽  
Author(s):  
Jiang Wang ◽  
Brian P. Cary ◽  
Peyton Beyer ◽  
Samuel H. Gellman ◽  
Daniel Weix

A new strategy for the synthesis of ketones is presented based upon the decarboxylative coupling of N-hydroxyphthalimide (NHP) esters with S-2-pyridyl thioesters. The reactions are selective for the cross-coupled product because NHP esters act as radical donors and the thioesters act as acyl donors. The reaction conditions are general and mild, with over 40 examples presented, including larger fragments and the 20-mer peptide Exendin(9-39) on solid support.


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>


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