Tetrahedron Letters

Concise total synthesis of 9-methoxystrobilurin A

H Uchiro, K Nagasawa, Y Aiba, S Kobayashi

Index: Uchiro, Hiromi; Nagasawa, Koh; Aiba, Yasuyuki; Kobayashi, Susumu Tetrahedron Letters, 2000 , vol. 41, # 21 p. 4165 - 4168

Full Text: HTML

Citation Number: 17

Abstract

9-Methoxystrobilurin A (1) was isolated by Anke and Steglich et al. in 1995 1 as a new and potent analogue of antifungal β-methoxyacrylates. 2 Structurally complicated strobilurin K (2) 1. and 3. and L (3) 6 were also isolated in 1996, and they have a unique triene moiety including two electron-rich and acid-sensitive methyl enol ethers as common substructures. Interestingly, this 9-methoxystrobilurin family was found to exhibit potent cytostatic activity toward human- ...

Related Articles:

Derivatives of the potent angiotensin converting enzyme inhibitor 5 (S)-benzamido-4-oxo-6-phenylhexanoyl-L-proline: effect of changes at postions 2 and 5 of the …

[Almquist; Crase; Jennings-White; Meyer; Hoefle; Smith; Essenburg; Kaplan Journal of Medicinal Chemistry, 1982 , vol. 25, # 11 p. 1292 - 1299]

More Articles...