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1)  methyl 12-bromo-13,14-oxofurazan-deisopropyldehydroabietate
12-溴-13,14-氧化呋咱脱异丙基脱氢松香酸甲酯
1.
Starting from dehydroabietic acid, which was purified from disproportionated rosin, three novel heterocycle compounds, methyl 12,13-oxofurazan-deisopropyldehydroabietate, methyl 12,13-furazan- deisopropyldehydroabietate and methyl 12-bromo-13,14-oxofurazan-deisopropyldehydroabietate were syn- thesized through several steps, such as methylation, bromination, nitration and cyclization.
以歧化松香为原料,将其纯化得到脱氢松香酸,然后经甲酯化、溴代、硝化、成环等步骤,合成了三个新型脱氢松香酸甲酯呋咱的衍生物12,13-氧化呋咱脱异丙基脱氢松香酸甲酯、12,13-呋咱脱异丙基脱氢松香酸甲酯、12-溴-13,14-氧化呋咱脱异丙基脱氢松香酸甲酯
2)  12-brom-13,14-oxifurazan methyl dehydroabietate
12-溴-13,14-脱氢松香酸甲酯氧化呋咱
1.
Synthesis and characterization of 12-brom-13,14-oxifurazan methyl dehydroabietate;
12-溴-13,14-脱氢松香酸甲酯氧化呋咱的合成与表征
3)  methyl 12,13-oxofurazan-deisopropyldehydroabietate
12,13-氧化呋咱脱异丙基脱氢松香酸甲酯
1.
Starting from dehydroabietic acid, which was purified from disproportionated rosin, three novel heterocycle compounds, methyl 12,13-oxofurazan-deisopropyldehydroabietate, methyl 12,13-furazan- deisopropyldehydroabietate and methyl 12-bromo-13,14-oxofurazan-deisopropyldehydroabietate were syn- thesized through several steps, such as methylation, bromination, nitration and cyclization.
以歧化松香为原料,将其纯化得到脱氢松香酸,然后经甲酯化、溴代、硝化、成环等步骤,合成了三个新型脱氢松香酸甲酯呋咱的衍生物12,13-氧化呋咱脱异丙基脱氢松香酸甲酯、12,13-呋咱脱异丙基脱氢松香酸甲酯、12-溴-13,14-氧化呋咱脱异丙基脱氢松香酸甲酯
4)  13-furazan-deisopropyldehydroabietate
13-呋咱脱异丙基脱氢松香酸甲酯
5)  methyl 7-carbonyl-12,13-oxifurazandehydroabietate
7-羰基-12,13-氧化呋咱脱氢松香酸甲酯
1.
After treating Ⅴ with sodium azide,methyl 7-carbonyl-12,13-oxifurazandehydroabietate (Ⅶ) was obtained by refluxing in toluene.
以歧化松香为原料,将其纯化得到脱氢松香酸,用硫酸二甲酯酯化后,通过12位溴代、7位氧化、13位硝化得到7-羰基-12-溴-13-硝基脱氢松香酸甲酯(Ⅴ),Ⅴ经过与叠氮化钠反应后,在甲苯中回流关环得到7-羰基-12,13-氧化呋咱脱氢松香酸甲酯(Ⅶ),Ⅶ再用三苯基膦脱氧得到7-羰基-12,13-呋咱脱氢松香酸甲酯Ⅷ,这两种产物的产率分别为83%和76%;产物经IR、1HNMR1、3CNMR和MS进行了表征。
6)  13-furazandehydroabietate
13-呋咱脱氢松香酸甲酯
1.
Ⅶ was further converted to methyl 7-carbonyl-12,13-furazandehydroabietate(Ⅷ) through reacting with tri.
以歧化松香为原料,将其纯化得到脱氢松香酸,用硫酸二甲酯酯化后,通过12位溴代、7位氧化、13位硝化得到7-羰基-12-溴-13-硝基脱氢松香酸甲酯(Ⅴ),Ⅴ经过与叠氮化钠反应后,在甲苯中回流关环得到7-羰基-12,13-氧化呋咱脱氢松香酸甲酯(Ⅶ),Ⅶ再用三苯基膦脱氧得到7-羰基-12,13-呋咱脱氢松香酸甲酯Ⅷ,这两种产物的产率分别为83%和76%;产物经IR、1HNMR1、3CNMR和MS进行了表征。
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