78344-67-9Relevant articles and documents
Construction of two vicinal quaternary carbons by asymmetric allylic alkylation: Total synthesis of hyperolactone C and (-)-biyouyanagin A
Du, Chao,Li, Liqi,Li, Ying,Xie, Zhixiang
supporting information; experimental part, p. 7853 - 7856 (2010/04/05)
Call on triple A: Palladium-catalyzed asymmetric allylic alkylation (Pd-AAA; see scheme) has enabled a concise and efficient synthesis of hyperolacto ne C and (-)-biyouyanagin A in only six (20% Overall yield) and seven (8% overall yield) steps, respectively. The enantiomers of these natural products were also prepared by exploiting the same methodology.
CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XXV. SYNTHESIS AND CYCLIZATION OF 2-DIAZO-1,5-DIARYL-1,3,5-PENTANETRIONES AND 2-DIAZO-5-ARYL-3,5-DIOXOPENTANOIC ESTERS
Andreichikov, Yu.S.,Gein, L.F.,Gein, V.L.
, p. 545 - 550 (2007/10/02)
2-Diazo-1,5-diaryl-1,3,5-pentanetriones and ethyl 2-diazo-5-aryl-3,5-dioxopentanoates were obtained in the reaction of 5-aryl-2,3-dihydro-2,3-furandiones with aroyldiazomethanes and diazoacetic ester.In some cases the formation of diazopentanetriones is a