1402610-95-0Relevant academic research and scientific papers
Stereoselective and catalytic access to β-enaminones: An entry to pyrimidines
Gayon, Eric,Szymczyk, Monika,Gérard, Hélène,Vrancken, Emmanuel,Campagne, Jean-Marc
, p. 9205 - 9220 (2012)
We describe herein a highly stereoselective access to Cbz-protected β-enaminones 2 based on the NaOH catalyzed rearrangement of propargylic hydroxylamines 1. The synthetic potential of these β-enaminones is illustrated in an original synthesis of pyrimidi
PD(II)-Catalyzed ligand-controlled synthesis of 2,3-dihydroisoxazole-4-carboxylates and bis(2,3-dihydroisoxazol-4-Yl)methanones
Ariyama, Tomohiro,Kusakabe, Taichi,Sato, Keita,Funatogawa, Mifuyu,Lee, Dong,Takahashi, Keisuke,Kato, Keisuke
, p. 512 - 528 (2017/04/10)
Pd(II)-catalyzed ligand-controlled switching between cyclization-carbonylation and cyclization-carbonylation-cyclization-coupling(CCC-coupling) reactions of propargylic N-hydroxylamines was investigated. The use of a [Pd(tfa)2(box)] catalyst in MeOH affor
Stereoselective and catalytic access to β-enaminones: An entry to pyrimidines
Gayon, Eric,Szymczyk, Monika,Vrancken, Emmanuel,Campagne, Jean-Marc,Gerard, Helene
, p. 9205 - 9220,16 (2012/12/11)
We describe herein a highly stereoselective access to Cbz-protected β-enaminones 2 based on the NaOH catalyzed rearrangement of propargylic hydroxylamines 1. The synthetic potential of these β-enaminones is illustrated in an original synthesis of pyrimidi
