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钯和铜催化合成新型胆烷氨基蒽醌钳形配体的方法。

Pd- and Cu-catalyzed approaches in the syntheses of new cholane aminoanthraquinone pincer-like ligands.

作者信息

Lukashev Nikolay V, Grabovyi Gennadii A, Erzunov Dmitry A, Kazantsev Alexey V, Latyshev Gennadij V, Averin Alexei D, Beletskaya Irina P

机构信息

Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1-3, Moscow, 119991, Russia.

出版信息

Beilstein J Org Chem. 2017 Mar 20;13:564-570. doi: 10.3762/bjoc.13.55. eCollection 2017.

DOI:10.3762/bjoc.13.55
PMID:28405236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5372750/
Abstract

Cu- and Pd-catalyzed arylation of aminocholanes has been described for the first time. While this Cu-catalyzed protocol provides high yields in reactions of aminocholanes with iodoarenes, Pd catalysis was found to be preferable for the reactions of aminocholanes with dichloroanthraquinones. UV-vis titration of bis(cholanylamino)anthraquinones with a series of cations demonstrated their high binding affinity to Cu, Al, and Cr.

摘要

首次报道了铜和钯催化的氨基胆甾烷的芳基化反应。虽然这种铜催化的方法在氨基胆甾烷与碘代芳烃的反应中能提供高产率,但发现钯催化对于氨基胆甾烷与二氯蒽醌的反应更具优势。用一系列阳离子对双(胆甾基氨基)蒽醌进行紫外可见滴定,结果表明它们对铜、铝和铬具有高结合亲和力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/fd8d373a7cfa/Beilstein_J_Org_Chem-13-564-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/55852bf24c45/Beilstein_J_Org_Chem-13-564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/5994d7978735/Beilstein_J_Org_Chem-13-564-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/323785cf5312/Beilstein_J_Org_Chem-13-564-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/12aa517964cf/Beilstein_J_Org_Chem-13-564-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/5574b05a1b23/Beilstein_J_Org_Chem-13-564-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/fd8d373a7cfa/Beilstein_J_Org_Chem-13-564-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/55852bf24c45/Beilstein_J_Org_Chem-13-564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/5994d7978735/Beilstein_J_Org_Chem-13-564-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/323785cf5312/Beilstein_J_Org_Chem-13-564-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/12aa517964cf/Beilstein_J_Org_Chem-13-564-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/5574b05a1b23/Beilstein_J_Org_Chem-13-564-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fb/5372750/fd8d373a7cfa/Beilstein_J_Org_Chem-13-564-g003.jpg

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