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A convergent total synthesis of mappicine ketone: A leading antiviral compound
Tetrahedron ( IF 2.1 ) Pub Date : 23 April 1999 , DOI: 10.1016/s0040-4020(99)00191-x J.S. Yadav , Sanjita Sarkar , S. Chandrasekhar
Tetrahedron ( IF 2.1 ) Pub Date : 23 April 1999 , DOI: 10.1016/s0040-4020(99)00191-x J.S. Yadav , Sanjita Sarkar , S. Chandrasekhar
An efficient total synthesis of the naturally occuring mappicine ketone 1 and mappicine 2 are described. The approach is based on the assembly of tricyclic amine 5 with pseudo acid chloride 20. A Friedlander condensation is utilized for the construction of the ABC skeleton and a periselective Diels-Alder approach is utilized for the preparation of the pseudo acid chloride.
中文翻译:
收敛的全合成甲氧苄啶酮:领先的抗病毒化合物
描述了天然存在的马卡比汀酮1和马卡比汀2的有效的全合成。该方法基于三环胺5与假酰氯20的组装。利用弗里德兰德缩合法来构建ABC骨架,并使用过选择性的Diels-Alder方法来制备假酰氯。
更新日期:2017-01-31
中文翻译:
收敛的全合成甲氧苄啶酮:领先的抗病毒化合物
描述了天然存在的马卡比汀酮1和马卡比汀2的有效的全合成。该方法基于三环胺5与假酰氯20的组装。利用弗里德兰德缩合法来构建ABC骨架,并使用过选择性的Diels-Alder方法来制备假酰氯。