Correction to “Regioselective Hydroboration of Unsymmetrical Internal Alkynes Catalyzed by a Cobalt Pincer-NHC Complex”

IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-10-10 DOI:10.1021/acs.orglett.4c03679
Naresh Kumar Meher, Maruti Suryavansi, K. Geetharani
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Abstract

We were made aware of an additional early discovery reported by Petit and co-workers on the cis-α-addition strategy for aryl-alkyl alkynes, which employed a phosphine-based ligand-substituted Cobalt-hydride catalyst. Thus, reference 10 in the original paper should be read as follows. (10) (a) Ferrand, L.; Lyu, Y.; Rivera-Hernández, A.; Fallon, B. J.; Amatore, M.; Aubert, C.; Petit, M. Hydroboration and Diboration of Internal Alkynes Catalyzed by a Well-Defined Low-Valent Cobalt Catalyst. Synthesis 2017, 49, 3895–3904.10.1055/s-0036-1588996. (b) Obligacion, J. V.; Neely, J. M.; Yazdani, A. N.; Pappas, I.; Chirik, P. J. Cobalt Catalyzed Z-Selective Hydroboration of Terminal Alkynes and Elucidation of the Origin of Selectivity. J. Am. Chem. Soc., 2015, 137, 5855–5858.10.1021/jacs.5b00936 (c) Ben-Daat, H.; Rock, C. L.; Flores, M.; Groy, T. L.; Bowman, A. C.; Trovitch, R. J. Hydroboration of alkynes and nitriles using an α-diimine cobalt hydride catalyst. Chem. Commun. 2017, 53, 7333–7336.10.1039/C7CC02281F (d) Zhang, G.; Wu, S.; Li, J.; Zeng, H.; Mo, Z.; Davis, K.; Zheng, S. Highly efficient and selective hydroboration of terminal and internal alkynes catalysed by a cobalt(II) coordination polymer. Org. Chem. Front. 2019, 6, 3228–3233.10.1039/C9QO00834A (e) González, M. J.; Bauer, F.; Breit, B. Cobalt-Catalyzed Hydroboration of Terminal and Internal Alkynes. Org. Lett. 2021, 23, 8199–8203.10.1021/acs.orglett.1c02854 (f) Blasius, C. K.; Vasilenko, V.; Matveeva, R.; Wadepohl, H.; Gade, L. H. Reaction Pathways and Redox States in α-Selective Cobalt-Catalyzed Hydroborations of Alkynes. Angew. Chem., Int. Ed. 2020, 59, 23010–23014.10.1002/anie.202009625 (g) Bories, C. C.; Sodreau, A.; Barbazanges, M.; Petit, M. Well-Defined Low-Valent Cobalt Complexes in Catalysis: An Overview. Organometallics, 2024, 43, 895–923.10.1021/acs.organomet.4c00054 This article has not yet been cited by other publications.
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对 "钴钳夹-NHC 复合物催化的不对称内部炔烃的区域选择性氢硼化反应 "的更正
我们还了解到 Petit 及其合作者在芳基-烷基炔的顺式-α-加成策略方面的早期发现,他们采用了一种基于膦的配体取代钴酸酐催化剂。因此,原论文中的参考文献 10 应理解如下。(10) (a) Ferrand, L.; Lyu, Y.; Rivera-Hernández, A.; Fallon, B. J.; Amatore, M.; Aubert, C.; Petit, M. Hydroboration and Diboration of Internal Alkynes Catalyzed by a Well-Defined Low-Valent Cobalt Catalyst.Synthesis 2017, 49, 3895-3904.10.1055/s-0036-1588996.(b) Obligacion, J. V.; Neely, J. M.; Yazdani, A. N.; Pappas, I.; Chirik, P. J. Cobalt Catalyzed Z-Selective Hydroboration of Terminal Alkynes and Elucidation of the Origin of Selectivity.J. Am.Chem.Soc., 2015, 137, 5855-5858.10.1021/jacs.5b00936 (c) Ben-Daat, H.; Rock, C. L.; Flores, M.; Groy, T. L.; Bowman, A. C.; Trovitch, R. J. Hydroboration of alkynes and nitriles using an α-diimine cobalt hydride catalyst.Chem.Chem.2017, 53, 7333-7336.10.1039/C7CC02281F (d) Zhang, G.; Wu, S.; Li, J.; Zeng, H.; Mo, Z.; Davis, K.; Zheng, S. Highly efficient and selective hydroboration of terminal and internal alkynes catalysed by a cobalt(II) coordination polymer.Org.Chem.Front.2019, 6, 3228-3233.10.1039/C9QO00834A (e) González, M. J.; Bauer, F.; Breit, B. Cobalt-Catalyzed Hydroboration of Terminal and Internal Alkynes.Org.Lett. 2021, 23, 8199-8203.10.1021/acs.orglett.1c02854 (f) Blasius, C. K.; Vasilenko, V.; Matveeva, R.; Wadepohl, H.; Gade, L. H. Reaction Pathways and Redox States in α-Selective Cobalt-Catalyzed Hydroborations of Alkynes.Angew.Chem.Ed.2020, 59, 23010-23014.10.1002/anie.202009625 (g) Bories, C. C.; Sodreau, A.; Barbazanges, M.; Petit, M. Well-Defined Low-Valent Cobalt Complexes in Catalysis:有机金属学》,2024 年,概述。Organometallics, 2024, 43, 895-923.10.1021/acs.organomet.4c00054 本文尚未被其他出版物引用。
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来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
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