Enantiomerically pure α-methoxyaryl acetaldehydes as versatile precursors: a facile chemo-enzymatic methodology for their preparation

التفاصيل البيبلوغرافية
العنوان: Enantiomerically pure α-methoxyaryl acetaldehydes as versatile precursors: a facile chemo-enzymatic methodology for their preparation
المؤلفون: Buddh Singh, Subhash C. Taneja, Asha Chaubey, Pankaj Gupta, Rajinder Parshad, Shiromani Sharma
المصدر: Tetrahedron: Asymmetry. 19:2579-2588
بيانات النشر: Elsevier BV, 2008.
سنة النشر: 2008
مصطلحات موضوعية: Acetonitriles, Chemistry, Arthrobacter sp, Organic Chemistry, Synthon, Acetaldehyde, Chemo enzymatic, Optically active, Catalysis, Kinetic resolution, Inorganic Chemistry, chemistry.chemical_compound, Organic chemistry, Physical and Theoretical Chemistry
الوصف: A facile and efficient synthesis of optically active α-methoxyaryl acetic acids (up to 95% ee), α-methoxyaryl ethanols (up to 93% ee) and α-methoxyaryl acetonitriles (up to 93% ee) was achieved via Arthrobacter sp. lipase-catalyzed kinetic resolution of masked aldehydes as the key synthons, that is, α-hydroxyaryl acetaldehyde acetals.
تدمد: 0957-4166
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2d598788ae26760755459c684eab0a6dTest
https://doi.org/10.1016/j.tetasy.2008.10.023Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........2d598788ae26760755459c684eab0a6d
قاعدة البيانات: OpenAIRE