Palladium-Catalyzed One-Pot Conversion of Aldehydes and Ketones into 4‑Substituted Homopropargyl Alcohols and 5‑En-3-yn-1-ols

 

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون: Umaña, Christian A., Cabezas Pizarro, Jorge A.
التنسيق: artículo original
تاريخ النشر:2017
الوصف:Sequential treatment of 2,3-dichloropropene with magnesium and n-BuLi generated the equivalent of 1,3- dilithiopropyne, which adds regiospecifically to aldehydes and ketones to produce homopropargyl alcohols. The lithium acetylide intermediate formed in this protocol can be further reacted with aromatic and vinyl halides, under palladium catalysis, to produce 4-substituted homopropargyl alcohols and 5-en-3-yn-1-ols, respectively, in one-pot with good overall yields.
البلد:Kérwá
المؤسسة:Universidad de Costa Rica
Repositorio:Kérwá
اللغة:Inglés
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/87985
الوصول للمادة أونلاين:https://pubs.acs.org/doi/10.1021/acs.joc.7b01529
https://hdl.handle.net/10669/87985
كلمة مفتاحية:Alcohols
Allenes
Aromatic compounds
Hydrocarbons
Palladium