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المؤلفون: Jieping Zhu, Taoues Laïb
المصدر: ResearcherID
مصطلحات موضوعية: intramol. cyclization, prepn. of meta-cyclophane structural cores of antimitotic phomopsins and ustiloxins), Metacyclophanes Role: SPN (Synthetic preparation), chemistry.chemical_compound, Chemistry, Stereochemistry, Nucleophilic aromatic substitution, phomopsin ustiloxin metacyclophane structural core prepn, Organic Chemistry, β elimination, Antimitotic Agent, Cyclization (SNAr, Mitosis (antimitotic agents, Substitution reaction (arom, PREP (Preparation) (prepn. of meta-cyclophane structural cores of antimitotic phomopsins and ustiloxins), Elimination reaction (beta, Cyclophane
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e56c6cebfec57096e76ae833b216c0
https://doi.org/10.1055/s-2000-7137 -
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المؤلفون: Xiaochuan Chen, Jieping Zhu
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
المصدر: Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2007, 46 (21), pp.3962-3965. ⟨10.1002/anie.200700539⟩مصطلحات موضوعية: Longest linear sequence, Stereochemistry, Cribrostatin-4, Molecular Conformation, 010402 general chemistry, 01 natural sciences, Catalysis, Domino, Biological Factors, chemistry.chemical_compound, Organic chemistry, Animals, Beta-Hydride elimination, Mannich reaction, ComputingMilieux_MISCELLANEOUS, Natural product, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Enantioselective synthesis, Total synthesis, cribrostatin asym total synthesis elimination intramol phenolic Mannich reaction, renieramycin asym total synthesis elimination intramol phenolic Mannich reaction, Stereoisomerism, General Chemistry, General Medicine, Isoquinolines, Porifera, 0104 chemical sciences, Mannich reaction (intramol, asym. total synthesis of the marine natural product (-)-cribrostatin 4 via beta elimination and an intramol. phenolic Mannich reaction), Stereoselective synthesis (total synthesis of the marine natural product (-)-cribrostatin 4 via beta elimination and an intramol. phenolic Mannich reaction), Elimination reaction (beta, chemistry, Yield (chemistry)