97185-46-1Relevant articles and documents
Mn(III)/Cu(II)-mediated oxidative radical cyclization of α-(methylthio)acetamides leading to erythrinanes
Chikaoka, Shiho,Toyao, Atsushi,Ogasawara, Mizuho,Tamura, Osamu,Ishibashi, Hiroyuki
, p. 312 - 318 (2007/10/03)
Treatment of N-[2-(3,4-dimethoxyphenyl)ethyl]-α-(methylthio)acetamide 3 with Mn(OAc)3 in the presence of Cu(Oac)2 gave tetrahydroindol-2-one 4, which then cyclized with Mn(Oac)3 to give 4-acetoxyerythrinane 5. A similar reaction of the 3,4-methylenedioxyphenyl congener 8 also gave tetrahydroindol-2-one 9, which, however, gave only a trace amount of the Mn(OAc)3-mediated cyclization product 11 and afforded the oxidation product 10. On the basis of these results, formation of 5 from 4 was thought to proceed via nucleophilic attack of the pyrrole ring on the cation-radical IX, generated by a single electron-transfer reaction of the acetoxy-substituted intermediate V. Treatment of compound 16 with Mn(OAc)3/Cu(OAc)2 gave no erythrinane derivative with recovery of the starting material, indicating that the presence of a methylthio group of 4 is essential for effecting the formation of erythrinane 5. On the other hand, treatment of 3 with Mn(OAc)3 using Cu(OTf)2 as an additive in place of Cu(OAc)2 gave another erythrinane 17. This method was applied to a formal synthesis of 3-demethoxyerythratidinone (20), a naturally occurring Erythrina alkaloid.
ACID-CATALYZED CYCLIZATIONS OF N-VINYL-α-SULFINYLACETAMIDES A NOVEL SYNTHETIC APPROACH TO ERYTHRINANE
Tamura, Y.,Maeda, H.,Akai, S.,Ishibashi, H.
, p. 2209 - 2212 (2007/10/02)
Under the Pummerer reaction conditions, N-(1-cyclohexenyl)-N-methyl-α-(methylsulfinyl)acetamide (7a) cyclized in a 5-endo trigonal fashion through the intermediary cation (8) to give the tetrahydro-4H-oxindole (10).The reaction was successively applied to a novel synthesis of erythrinane skeleton.
