دورية أكاديمية

Enantioselective Au( i )-catalyzed tandem reactions between 2-alkynyl enones and naphthols by the tethered counterion-directed catalysis strategy

التفاصيل البيبلوغرافية
العنوان: Enantioselective Au( i )-catalyzed tandem reactions between 2-alkynyl enones and naphthols by the tethered counterion-directed catalysis strategy
المؤلفون: Yu, Yunliang, Sabat, Nazarii, Daghmoum, Meriem, Zhang, Zhenhao, Retailleau, Pascal, Frison, Gilles, Marinetti, Angela, Guinchard, Xavier
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie - CNRS Chimie (INC-CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO), Laboratoire de chimie moléculaire (LCM), École polytechnique (X)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie théorique (LCT), Institut de Chimie - CNRS Chimie (INC-CNRS)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), ANR-20-CE07-0037,BiAuCat,L'âge doré de la biocatalyse: Combiner des Enzymes et de l'Au(I)(2020)
المصدر: ISSN: 2052-4110.
بيانات النشر: HAL CCSD
Royal Society of Chemistry
سنة النشر: 2023
مصطلحات موضوعية: [CHIM.ORGA]Chemical Sciences/Organic chemistry, [CHIM.CATA]Chemical Sciences/Catalysis
الوصف: International audience ; Enantioselective tandem cycloisomerization/addition reactions of 2-alkynyl enones with 1- and 2-naphthols have been investigated using gold(I) catalysts featuring hybrid phosphine–phosphoric acid chiral ligands, according to the tethered counterion-directed catalysis (TCDC) strategy. The reactions occur at low catalyst loading (0.2–1 mol%) without silver additives, and the naphthols act as both O- and C-nucleophiles, leading to the corresponding addition products with high enantioselectivity. DFT calculations enlighten these processes
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: hal-04220207; https://hal.science/hal-04220207Test; https://hal.science/hal-04220207/documentTest; https://hal.science/hal-04220207/file/draft%20ChemRxiv.pdfTest; CHEMRXIV: 10.26434/chemrxiv-2023-s8hq5
DOI: 10.1039/D3QO00415E
الإتاحة: https://doi.org/10.1039/D3QO00415ETest
https://hal.science/hal-04220207Test
https://hal.science/hal-04220207/documentTest
https://hal.science/hal-04220207/file/draft%20ChemRxiv.pdfTest
حقوق: info:eu-repo/semantics/OpenAccess
رقم الانضمام: edsbas.722C18F2
قاعدة البيانات: BASE