Highly efficient Pd‐PEPPSI‐IPr catalyst for  N ‐(4‐pyridazinyl)‐bridged bicyclic sulfonamides via Suzuki–Miyaura coupling reaction | Zendy

Sura Mallikarjuna Reddy | Zendy; Bijivemula N. Reddy | Zendy; Pogula Sreekanth Reddy | Zendy; Motakatla Venkata Krishna Reddy | Zendy; Madhvesh Pathak | Zendy; Peddiahgari Vasu Govardhana Reddy | Zendy

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Highly efficient Pd‐PEPPSI‐IPr catalyst for N ‐(4‐pyridazinyl)‐bridged bicyclic sulfonamides via Suzuki–Miyaura coupling reaction

Author(s) -

Sura Mallikarjuna Reddy,

Bijivemula N. Reddy,

Pogula Sreekanth Reddy,

Motakatla Venkata Krishna Reddy,

Madhvesh Pathak,

Peddiahgari Vasu Govardhana Reddy

Publication year - 2018

Publication title -

applied organometallic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.53

H-Index - 71

eISSN - 1099-0739

pISSN - 0268-2605

DOI - 10.1002/aoc.4068

Subject(s) - chemistry , catalysis , aryl , suzuki reaction , bicyclic molecule , coupling reaction , coupling (piping) , combinatorial chemistry , organic chemistry , palladium , medicinal chemistry , metallurgy , alkyl , materials science

A protocol for the Suzuki–Miyaura coupling of novel 2‐(6‐chloropyridazin‐3‐yl)‐5‐(aryl/heteroarylsulfonyl)‐2,5‐diazabicyclo[2.2.1]heptanes and heteroarylboronic acids to afford variety of coupled products was realized. Pd‐PEPPSI‐IPr catalyst was found to be a powerful and reusable catalyst under relatively mild reaction conditions.

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