TY - JOUR
T1 - Bedford-type palladacycle catalyzed Miyaura-borylation of aryl halides with tetrahydroxydiboron in water
AU - Zernickel, Anna
AU - du, weiyuan
AU - Ghorpade, Seema
AU - Sawant, Dinesh
AU - Makki, Arwa
AU - Sekar, Nagaiyan
AU - Eppinger, Jörg
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): FIC/2010/07
Acknowledgements: This work was supported by the King Abdullah University of Science and Technology (KAUST baseline funding and GCR grant FIC/2010/07). Authors are gratefully acknowledging support from King Abdullah University of Science and Technology (KAUST), Saudi Arabia.
PY - 2018/1/30
Y1 - 2018/1/30
N2 - A mild aqueous protocol for palladium catalyzed Miyaura borylation of aryl iodides, aryl bromides and aryl chlorides with tetrahydroxydiboron (BBA) as a borylating agent is developed. The developed methodology requires low catalyst loading of Bedford-type palladacycle catalyst (0.05 mol %) and works best under mild reaction conditions at 40 °C in short time of 6 hours in water. In addition, our studies show that for Miyaura borylation using BBA in aqueous condition, maintaining a neutral reaction pH is very important for reproducibility and higher yields of corresponding borylated products. Moreover, our protocol is applicable for a broad range of aryl halides, corresponding borylated products are obtained in excellent yields up to 93% with 29 examples demonstrating its broad utility and functional group tolerance.
AB - A mild aqueous protocol for palladium catalyzed Miyaura borylation of aryl iodides, aryl bromides and aryl chlorides with tetrahydroxydiboron (BBA) as a borylating agent is developed. The developed methodology requires low catalyst loading of Bedford-type palladacycle catalyst (0.05 mol %) and works best under mild reaction conditions at 40 °C in short time of 6 hours in water. In addition, our studies show that for Miyaura borylation using BBA in aqueous condition, maintaining a neutral reaction pH is very important for reproducibility and higher yields of corresponding borylated products. Moreover, our protocol is applicable for a broad range of aryl halides, corresponding borylated products are obtained in excellent yields up to 93% with 29 examples demonstrating its broad utility and functional group tolerance.
UR - http://hdl.handle.net/10754/626747
UR - http://pubs.acs.org/doi/10.1021/acs.joc.7b02771
UR - http://www.scopus.com/inward/record.url?scp=85042196553&partnerID=8YFLogxK
U2 - 10.1021/acs.joc.7b02771
DO - 10.1021/acs.joc.7b02771
M3 - Article
C2 - 29313348
SN - 0022-3263
VL - 83
SP - 1842
EP - 1851
JO - The Journal of Organic Chemistry
JF - The Journal of Organic Chemistry
IS - 4
ER -