Stereoselective Diversity-Oriented Solution and Solid-Phase Synthesis of Tetrahydroquinoline-Based Polycyclic Derivatives

التفاصيل البيبلوغرافية
العنوان: Stereoselective Diversity-Oriented Solution and Solid-Phase Synthesis of Tetrahydroquinoline-Based Polycyclic Derivatives
المؤلفون: Reni Joseph, Patricia Durieux, Donald M. Leek, Prabhat Arya, Zai-Xin Chen
المصدر: Journal of Combinatorial Chemistry. 6:54-64
بيانات النشر: American Chemical Society (ACS), 2003.
سنة النشر: 2003
مصطلحات موضوعية: Spectrometry, Mass, Electrospray Ionization, Magnetic Resonance Spectroscopy, Bicyclic molecule, Chemistry, Stereoisomerism, Borohydrides, General Chemistry, Solution synthesis, Metathesis, Combinatorial chemistry, Solutions, Enantiopure drug, Solid-phase synthesis, Lithium Compounds, Quinolines, Michael reaction, Organic chemistry, Indicators and Reagents, Polycyclic Compounds, Stereoselectivity
الوصف: A diversity-oriented solution and solid-phase synthesis of tetrahydroquinoline-based tricyclic derivatives has been achieved from enantiomerically pure, natural product-like bicyclic scaffold. The solution synthesis of enantiopure bicyclic scaffold was developed by asymmetric hetero Michael reaction. Our approach for the synthesis of polycyclic derivatives utilized regio- and stereoselective hetero Michael reaction and ring-closing metathesis as key steps in solution and on solid phase.
وصف الملف: application/pdf
تدمد: 1520-4774
1520-4766
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5e294169544e585714beb22dba405d
https://doi.org/10.1021/cc034053z
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....da5e294169544e585714beb22dba405d
قاعدة البيانات: OpenAIRE