93946-59-9Relevant academic research and scientific papers
Electrophilic-induced cyclization reaction of hexahydroindolinone derivatives and its application toward the synthesis of (±)- erysotramidine
Padwa, Albert,Lee, Hyoung Ik,Rashatasakhon, Paitoon,Rose, Mickea
, p. 8209 - 8218 (2007/10/03)
A convenient synthesis of variously substituted octahydroindolo[7a,1a]- isoquinolinones has been achieved by an acid-induced cyclization of hexahydroindolinones bearing tethered phenethyl groups. The formation of a single lactam diastereomer is the result
Efficient synthesis of (+/-)-erysotramidine using an NBS-promoted cyclization reaction of a hexahydroindolinone derivative.
Lee, Hyoung Ik,Cassidy, Michael P,Rashatasakhon, Paitoon,Padwa, Albert
, p. 5067 - 5070 (2007/10/03)
An NBS-promoted intramolecular electrophilic aromatic substitution reaction of a hexahydroindolinone derivative was used to assemble the tetracyclic core of the erythrinane skeleton. The resulting cyclized product was transformed into (+/-)-erysotramidine
