Correction to “Nickel-Catalyzed Asymmetric Reductive Aryl-Benzylation of Unactivated Alkenes”
نویسندگان
چکیده
ADVERTISEMENT RETURN TO ISSUEPREVAddition/CorrectionNEXTORIGINAL ARTICLEThis notice is a correctionCorrection to “Nickel-Catalyzed Asymmetric Reductive Aryl-Benzylation of Unactivated Alkenes”Youxiang JinYouxiang JinMore by Youxiang Jin, Haobo YangHaobo YangMore Yang, and Chuan Wang*Chuan WangMore Wanghttp://orcid.org/0000-0002-9219-1785Cite this: Org. Lett. 2021, 23, 9, 3798Publication Date (Web):April 13, 2021Publication History Received31 March 2021Published online13 April inissue 7 May 2021https://doi.org/10.1021/acs.orglett.1c01098Copyright © 2021 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views779Altmetric-Citations-LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum full text article downloads since November 2008 (both PDF HTML) across all institutions individuals. These metrics regularly updated reflect usage leading up last few days.Citations number other articles citing this article, calculated Crossref daily. Find more information about citation counts.The Altmetric Attention Score quantitative measure attention that research has received online. Clicking on donut icon will load page at altmetric.com with additional details score social media presence for given article. how calculated. Share Add toView InAdd Full Text ReferenceAdd Description ExportRISCitationCitation abstractCitation referencesMore Options onFacebookTwitterWechatLinked InReddit (424 KB) Get e-Alerts
منابع مشابه
Rhodium-catalyzed asymmetric intramolecular hydroamination of unactivated alkenes.
Metal-catalyzed enantioselective intramolecular hydroamination of olefins1 is one of the most conceptually simple and atom-economical approaches to the construction of enantioenriched nitrogen heterocycles,2 which are valuable synthons in the preparation of natural products and biologically active molecules.3 Despite significant advances,4,5,6 no general solution for this challenging transforma...
متن کاملPalladium-catalyzed asymmetric benzylation of 3-aryl oxindoles.
Herein we report palladium-catalyzed asymmetric benzylic alkylation with 3-aryl oxindoles as prochiral nucleophiles. Proceeding analogously to asymmetric allylic alkylation, asymmetric benzylation occurs in high yield and enantioselectivity for a variety of unprotected 3-aryl oxindoles and benzylic methyl carbonates using chiral bisphosphine ligands. This methodology represents a novel asymmetr...
متن کاملNickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes.
An asymmetric Ni-catalyzed reductive cross-coupling of (hetero)aryl iodides and benzylic chlorides has been developed to prepare enantioenriched 1,1-diarylalkanes. As part of these studies, a new chiral bioxazoline ligand, 4-heptyl-BiOX (L1), was developed in order to obtain products in synthetically useful yield and enantioselectivity. The reaction tolerates a variety of heterocyclic coupling ...
متن کاملNickel-catalyzed reductive allylation of aryl bromides with allylic acetates.
This paper highlights Ni-catalyzed allylation of electron-rich aryl bromides with a variety of substituted allylic carbonates using zinc as the terminal reductant, affording E-alkenes regioselectively in good to excellent yields by the addition of aryl to the less hindered allylic carbon. The electron-deficient aryl bromides and chlorides are also highly efficient coupling partners.
متن کاملCopper-catalyzed oxytrifluoromethylation of unactivated alkenes.
A mild, versatile, and convenient method for the efficient oxytrifluoromethylation of unactivated alkenes based on a copper-catalyzed oxidative difunctionalization strategy has been developed. This methodology provides access to a variety of classes of synthetically useful CF(3)-containing building blocks from simple starting materials.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Organic Letters
سال: 2021
ISSN: ['1523-7060', '1523-7052']
DOI: https://doi.org/10.1021/acs.orglett.1c01098