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Total synthesis of rodgersinine A and B
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作者 苗强 谢新刚 +2 位作者 张基勇 厍学功 潘鑫复 《Journal of Chinese Pharmaceutical Sciences》 CAS 2007年第1期41-42,共2页
Aim Syntheses of benzodioxane neolignans. Method The SN2 reaction and Corey-Fuchs reaction was used to synthesize Rodgersinine A, 4-[3-methyl-7-[(E)-1-propenyl-2, 3-dihydro-1, 4-benzodioxin-2-yl]-l, 2-benzenediol (... Aim Syntheses of benzodioxane neolignans. Method The SN2 reaction and Corey-Fuchs reaction was used to synthesize Rodgersinine A, 4-[3-methyl-7-[(E)-1-propenyl-2, 3-dihydro-1, 4-benzodioxin-2-yl]-l, 2-benzenediol (1) and Rodgersinine B, 4- [3-methyl- 7-(1-propynyl)-2, 3-dihydro- 1, 4-benzodioxin-2-yl]-0, 2-benzenediol (2). Results Total synthesis ofRodgersinine A and B was first completed. Conclusion A useful method for constructing benzodioxane neolignans by the SN2 reaction is achieved. 展开更多
关键词 Corey-Fuchs reaction closed ring by acid SN2 reaction Acetylenic functionality
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