scholarly journals Stereoselective Formation of Trisubstituted Vinyl Boronate Esters by the Acid-Mediated Elimination of α-Hydroxyboronate Esters

2014 ◽  
Vol 79 (15) ◽  
pp. 7199-7204 ◽  
Author(s):  
Weiye Guan ◽  
Alicia K. Michael ◽  
Melissa L. McIntosh ◽  
Liza Koren-Selfridge ◽  
John P. Scott ◽  
...  
Keyword(s):  
Boronate Esters

Suzuki coupling of Aroyl-MIDA boronate esters – a Preliminary report on Scope and Limitations

2021 ◽  
pp. 153147
Author(s):  
Samson Lai ◽  
Noah Takaesu ◽  
Wen Xuan Lin ◽  
David M. Perrin
Keyword(s):  
Preliminary Report ◽  
Suzuki Coupling ◽  
Boronate Esters

Platinum pyridinecarboxaldimine complexes containing boronate esters

2004 ◽  
Vol 82 (12) ◽  
pp. 1692-1699 ◽  
Author(s):  
Hanni A Darwish ◽  
Stephen J Scales ◽  
Jennifer L Horton ◽  
Liliya G Nikolcheva ◽  
Haiwen Zhang ◽  
...  
Keyword(s):  
Ovarian Carcinoma ◽  
Key Words ◽  
Cell Line ◽  
Platinum Complexes ◽  
Resistant Cell ◽  
Resistant Cell Line ◽  
Boronate Esters ◽  
Human Ovarian Carcinoma

Condensation of 2-pyridinecarboxaldehydes with 2-, 3-, and 4-H2NC6H4Bpin (pin = 1,2-O2C2Me4) gave the corresponding boron-containing pyridinecarboxaldimines (N–NBpin). Addition of these ligands to [PtCl2(coe)]2 (coe = cis-cyclooctene) gave complexes of the type cis-PtCl2(N–NBpin) in moderate yields. The platinum complexes have been examined for their potential cytotoxicities against OV2008 (human ovarian carcinoma) and the analogous cisplatin-resistant cell line C13. Key words: boronate esters, pyridinecarboxaldimines, cytotoxicity, platinum, boron.

ChemInform Abstract: Harnessing C-H Borylation/Deborylation for Selective Deuteration, Synthesis of Boronate Esters, and Late Stage Functionalization.

ChemInform ◽  
2016 ◽  
Vol 47 (4) ◽  
pp. no-no
Author(s):  
Venkata A Kallepalli ◽  
Kristin A. Gore ◽  
Feng Shi ◽  
Luis Sanchez ◽  
Ghayoor A. Chotana ◽  
...  
Keyword(s):  
Late Stage ◽  
Boronate Esters ◽  
Selective Deuteration

scholarly journals Formation of C(sp2)Boronate Esters by Borylative Cyclization of Alkynes Using BCl3

2015 ◽  
Vol 127 (38) ◽  
pp. 11397-11401 ◽  
Author(s):  
Andrew J. Warner ◽  
James R. Lawson ◽  
Valerio Fasano ◽  
Michael J. Ingleson
Keyword(s):  
Boronate Esters

RhIII-catalyzed heteroarylation of N-2,6-difluorophenyl arylamides with heteroaryl boronate esters

2022 ◽  
Author(s):  
Jia-Xue Wu ◽  
Qing-Xia Yao ◽  
Wen-zeng Duan ◽  
DaCheng Li ◽  
Xianqiang Huang ◽  
...  
Keyword(s):  
Boronate Esters ◽  
Efficient Strategy ◽  
Directing Group

Herein, an efficient strategy to aryl-heteroaryl formation via RhIII-catalyzed ortho-C(sp2)−H heteroarylation of (hetero)arenes with heterocyclic boronates using a readily removable N-2,6-difluorophenyl arylamides directing group has been disclosed. A variety of...

Boronate ester post-functionalization of PPEs: versatile building blocks for poly(2,2′-(1-(4-(1,2-di(thiophen-2-yl)vinyl)phenyl)-2-(2,5-dioctylphenyl)ethene-1,2-diyl)dithiophene) and application in field effect transistors

2015 ◽  
Vol 3 (39) ◽  
pp. 10074-10078 ◽  
Author(s):  
Junwei Yang ◽  
Moyun Chen ◽  
Ji Ma ◽  
Wei Huang ◽  
Haoyun Zhu ◽  
...  
Keyword(s):  
Field Effect ◽  
Field Effect Transistors ◽  
Building Blocks ◽  
Boronate Esters ◽  
Boronate Ester ◽  
Post Functionalization

Novel boronate esters synthesized by the post-functionalization of PPEs and oligomers can provide an versatile platform for analogues.

Synthesis and effective catalytic performance in cycloaddition reactions with CO2 of boronate esters versus N-heterocyclic carbene (NHC)-stabilized boronate esters

2020 ◽  
Vol 4 (11) ◽  
pp. 5682-5696
Author(s):  
Ahmet Kilic ◽  
Bayram Sobay ◽  
Emine Aytar ◽  
Rahime Söylemez
Keyword(s):  
Catalytic Performance ◽  
Cycloaddition Reactions ◽  
Cyclic Carbonates ◽  
Boronate Esters

New boronate esters were prepared and used as catalysts for the synthesis of cyclic carbonates from CO2 and epoxides without solvent.

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