PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
October 23, 2009Chemistry - A European Journal140 citations

Microwave‐Promoted Palladium(II)‐Catalyzed CP Bond Formation by Using Arylboronic Acids or Aryltrifluoroborates

View Full Paper
MAMounir AndaloussiJLJonas LindhJSJonas Sävmarker

Key Points

Key points are not available for this paper at this time.

Abstract

The first Pd(II)-catalyzed P arylation has been performed by using palladium acetate, the rigid bidentate ligand dmphen (dmphen=2,9-dimethyl-1,10-phenanthroline), and without the addition of base or acid. Couplings of arylboronic acids or aryl trifluoroborates with H-phosphonate dialkyl esters were conducted in 30 min with controlled microwave (MW) heating under non-inert conditions. Aryl phosphites were also synthesized at room temperature with atmospheric air as the sole reoxidant. The arylated phosphonates were isolated in 44-90 % yields. The excellent chemoselectivity of the method was illustrated in the synthesis of a Mycobacterium tuberculosis glutamine synthetase (MTB-GS) inhibitor. Online ESIMS was used to detect cationic palladium species in ongoing reactions directly, and a catalytic cycle has been proposed based on these results.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Andaloussi et al. (2009) studied this question.

synapsesocial.com/papers/6a9227232844244f4b1b45edhttps://doi.org/10.1002/chem.200901473
Ask AI
Helpful
Bookmark
Share
View Full Paper