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机译:通过形式的[2 + 2 + 2]环状结构构筑具有多个手性中心的六元螺环氧化吲哚的有机催化串联反应
Key Laboratory of Drug-Targeting and Drug Delivery System of Education Ministry, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu, 610041 (China), Fax: (+86)
28-85502609;
Key Laboratory of Drug-Targeting and Drug Delivery System of Education Ministry, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu, 610041 (China), Fax: (+86)
28-85502609;
Key Laboratory of Drug-Targeting and Drug Delivery System of Education Ministry, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu, 610041 (China), Fax: (+86)
28-85502609;
Key Laboratory of Drug-Targeting and Drug Delivery System of Education Ministry, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu, 610041 (China), Fax: (+86)
28-85502609;
Key Labo;
annulation; asymmetric catalysis; molecular complexity; spiro compounds; tandem reactions;
机译:通过形式的[2 + 2 + 2]环状结构构筑具有多个手性中心的六元螺环氧化吲哚的有机催化串联反应
机译:有机催化,不对称[2 + 2 + 2]环构造具有六个连续立体中心的六元螺环氧化吲哚。
机译:有机催化正式[5 + 1]环空:通过Michael-aldol反应的功能化六元螺环茚满-1,3-二酮/羟吲哚的非对映选择性级联合成
机译:与新型手性高效碘化物(摘要)有机催化反应
机译:钯催化和碘介导的正式[4 + 1]环空方案的开发。向羰基α-官能化的新的基于富烯的有机催化平台的进展。
机译:通过分子内Heck反应形成螺旋环吲哚的非对映选择性
机译:有机催化,不对称[2 + 2 + 2]环化构建6个连续立体中心的六元螺环氧吲哚