154417-83-1Relevant articles and documents
Thermal ene reaction of 4-(2-alkenylamino)-3-formyl-2(2H)-chromenones
Kuroki,Kuroki, Yoshiaki,Akao,Akao, Ryosuke,Inazumi,Inazumi, Tomonori,Noguchi,Noguchi, Michihiko
, p. 1063 - 1072 (2007/10/02)
Intramolecular ene reaction of 4-(2-alkenylamino)-3-formyl-2(2H)- chromenones 7 involving carbonyl enophile proceeded stereoselectively to afford 5-hydroxychromen[3,4-b]-azepines 14. The intramolecular nucleophilic attack of hydroxy group to the enemine moiety in 14 gave 1,2-dihydro-2,4- ethanochromen[4,3-d][1,3]oxazin-5(4H,5H)-one derivatives 13 as final products. PM3 MO calculations of the process reveal that this ene reaction proceeds with two steps through an intermediate.