erythbidin E 、 乙酸酐 在
吡啶 作用下,
以10 mg的产率得到[3-Acetyloxy-4-(6-methoxy-1-benzofuran-2-yl)phenyl] acetate
参考文献:
名称:
New Constituents from the Roots of Erythrina x bidwillii
摘要:
Three new compounds, erythbidins C-E (1-3), together with five known compounds 4-8 were isolated from the roots of Erythrina x bidwillii. Their structures were established on the basis of spectroscopic evidence. Among the isolated compounds, erythbidin E (3) showed a potent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA).
An environmentallyfriendly one-pot synthesis of 2-arylbenzofurans under ambient temperature has been developed. It features an ortho-hydroxyl group assisted Wittig reaction of substituted salicylaldehyde followed by an in situ oxidative cyclization. Its advantages include readily available and non-hazardous materials, benign reaction conditions (room temperature, green solvent and one-pot manner), easy work-up and high overall yields. Utilizing this methodology, various 2-aryl-benzofurans including four natural products have been synthesized.
Three new compounds, erythbidins C-E (1-3), together with five known compounds 4-8 were isolated from the roots of Erythrina x bidwillii. Their structures were established on the basis of spectroscopic evidence. Among the isolated compounds, erythbidin E (3) showed a potent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA).