Palladium‐Catalyzed Carbonylative Coupling Reactions of  N , N ‐Bis(methanesulfonyl)amides through C–N Bond Cleavage | Zendy

Lim Minkyung | Zendy; Kim Hyeji | Zendy; Ban Jaeyoung | Zendy; Son Junghan | Zendy; Lee Jae Kyun | Zendy; Min SunJoon | Zendy; Lee Sang Uck | Zendy; Rhee Hakjune | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Palladium‐Catalyzed Carbonylative Coupling Reactions of N , N ‐Bis(methanesulfonyl)amides through C–N Bond Cleavage

Author(s) -

Lim Minkyung,

Kim Hyeji,

Ban Jaeyoung,

Son Junghan,

Lee Jae Kyun,

Min SunJoon,

Lee Sang Uck,

Rhee Hakjune

Publication year - 2018

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201801124

Subject(s) - chemistry , palladium , cleavage (geology) , catalysis , aryl , bond cleavage , carbonylation , amide , medicinal chemistry , coupling reaction , substrate (aquarium) , organic chemistry , carbon monoxide , alkyl , oceanography , geotechnical engineering , fracture (geology) , engineering , geology

Palladium‐catalyzed carbonylative coupling reactions of various N , N ‐bis(methanesulfonyl)amides with arylboronic acids through C–N bond cleavage were carried out. The reactions proceeded under mild conditions in a short period of time without any additives to afford a wide range of unsymmetrical aryl ketones in excellent yields. This is the first example of a carbonylative coupling reaction using N , N ‐bis(methanesulfonyl)amide as a coupling substrate.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research