641-92-9Relevant academic research and scientific papers
SYNTHESIS OF ξ-PYRROMYCINONE, 7-DEOXYAURAMYCINONE, AND 7-DEOXYAKLAVINONE VIA KETOESTER CYCLIZATION
Krohn, Karsten,Klimars, Michael,Koehle, Hans-Juergen,Ebeling, Eckehardt
, p. 3677 - 3694 (1984)
7,10-O-Dimethyl-ξ-pyrromycinone (78) and the not naturally occurring 7-deoxyanthracyclinones 76 and 77 are prepared via base induced cyclization of the ketoesters 73-75, and stereoselectively hydroxylated to the 2,4-cis diols 83 and 85.
Regiospecific Total Syntheses of (+/-)-Aklavinone and (+/-)-ε-Pyrromycinone from a Common Synthon
Hauser, Frank M.,Mal Dipakranjan
, p. 1098 - 1104 (2007/10/02)
The preparation and use of cyclohexenone 10 as a common intermediate for regiospecific total synthesis of both (+/-)-aklavinone (1a) and (+/-)-ε-pyrromycinone (2a) is described.
