Ellipticine analogs: oxygen and sulfur isosteres

AN Fujiwara, EM Acton…

Index: Fujiwara,A.N. et al. Journal of Heterocyclic Chemistry, 1969 , vol. 6, p. 379 - 387

Full Text: HTML

Citation Number: 16

Abstract

Abstract Oxaellipticine has been synthesized from 1, 4-dimethyldibenzofuran, by converting it to the 2-aldehyde, forming the Schiff's base with aminoacetaldehyde diethyl acetal, and cyclizing this with 105% superphosphoric acid. Alternatively, tetrahydrodimethyldibenzofuran was formylated mainly at the 3-position, and the 3-(2- nitrovinyl) derivative of the 3-aldehyde, by hydride reduction, then Bischler-Napieralski ...

Related Articles:

Synthesis of 6-thiaellipticine and related compounds via heterocyclic o-quinodimethane intermediates

[Kano, Shinzo; Mochizuki, Naoki; Hibino, Satoshi; Shibuya, Shiroshi Journal of Organic Chemistry, 1982 , vol. 47, # 18 p. 3566 - 3569]

More Articles...