{"title":"整洁条件下4 A0分子筛介导间甲酚与手性胺的立体选择性氨基甲基化反应","authors":"M. Gholizadeh","doi":"10.2174/1876214X00902010054","DOIUrl":null,"url":null,"abstract":"A minomethylation at ortho position with respect to hydroxyl group of mcresol in presence carefully dried 4A molecular sieves under neat conditions. One pot, two component,Mannich reaction of m-cresol with imine at 600C temperature under solvent free conditions affords the corresponding aminomethylated products in good yields, with moderate stereoselectivity.","PeriodicalId":22755,"journal":{"name":"The Open Catalysis Journal","volume":"23 1","pages":"54-60"},"PeriodicalIF":0.0000,"publicationDate":"2009-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stereoselective Aminomethylation of m-Cresol with Chiral Amine Mediated by 4 A0 Molecular Sieves Under Neat Conditions\",\"authors\":\"M. Gholizadeh\",\"doi\":\"10.2174/1876214X00902010054\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A minomethylation at ortho position with respect to hydroxyl group of mcresol in presence carefully dried 4A molecular sieves under neat conditions. One pot, two component,Mannich reaction of m-cresol with imine at 600C temperature under solvent free conditions affords the corresponding aminomethylated products in good yields, with moderate stereoselectivity.\",\"PeriodicalId\":22755,\"journal\":{\"name\":\"The Open Catalysis Journal\",\"volume\":\"23 1\",\"pages\":\"54-60\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Open Catalysis Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/1876214X00902010054\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Catalysis Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1876214X00902010054","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Stereoselective Aminomethylation of m-Cresol with Chiral Amine Mediated by 4 A0 Molecular Sieves Under Neat Conditions
A minomethylation at ortho position with respect to hydroxyl group of mcresol in presence carefully dried 4A molecular sieves under neat conditions. One pot, two component,Mannich reaction of m-cresol with imine at 600C temperature under solvent free conditions affords the corresponding aminomethylated products in good yields, with moderate stereoselectivity.