Correction to "Conformational Flexibility as a Tool for Enabling Site-Selective Functionalization of Unactivated C-O Bonds in Cyclic Acetals".
作者信息
Romano Ciro, Talavera Laura, Gómez-Bengoa Enrique, Martin Ruben
出版信息
J Am Chem Soc. 2022 Aug 17;144(32):14959. doi: 10.1021/jacs.2c07724. Epub 2022 Aug 4.
Abstract
摘要
相似文献
1
Correction to "Conformational Flexibility as a Tool for Enabling Site-Selective Functionalization of Unactivated C-O Bonds in Cyclic Acetals".
J Am Chem Soc. 2022 Aug 17;144(32):14959. doi: 10.1021/jacs.2c07724. Epub 2022 Aug 4.
2
Conformational Flexibility as a Tool for Enabling Site-Selective Functionalization of Unactivated C-O Bonds in Cyclic Acetals.
J Am Chem Soc. 2022 Jul 6;144(26):11558-11563. doi: 10.1021/jacs.2c04513. Epub 2022 Jun 24.
3
2-(Pyridin-2-yl)isopropyl (PIP) Amine: An Enabling Directing Group for Divergent and Asymmetric Functionalization of Unactivated Methylene C(sp)-H Bonds.
Acc Chem Res. 2021 Jun 15;54(12):2750-2763. doi: 10.1021/acs.accounts.1c00168. Epub 2021 May 21.
4
Intramolecular, Site-Selective, Iodine-Mediated, Amination of Unactivated (sp)C-H Bonds for the Synthesis of Indoline Derivatives.
Org Lett. 2017 Jun 2;19(11):2793-2796. doi: 10.1021/acs.orglett.7b00846. Epub 2017 May 16.
5
Copper-catalyzed site-selective intramolecular amidation of unactivated C(sp³)-H bonds.
Angew Chem Int Ed Engl. 2014 Apr 1;53(14):3706-10. doi: 10.1002/anie.201311263. Epub 2014 Mar 3.
6
Nickel-catalyzed site-selective amidation of unactivated C(sp(3))-H bonds.
Chemistry. 2014 Jul 28;20(31):9530-3. doi: 10.1002/chem.201403356. Epub 2014 Jun 25.
7
Copper-promoted site-selective acyloxylation of unactivated C(sp³)-H bonds.
Chem Asian J. 2014 Oct;9(10):2736-9. doi: 10.1002/asia.201402510. Epub 2014 Jul 24.
8
Copper-Catalyzed Intermolecular Functionalization of Unactivated C(sp)-H Bonds and Aliphatic Carboxylic Acids.
J Am Chem Soc. 2021 Sep 15;143(36):14667-14675. doi: 10.1021/jacs.1c05874. Epub 2021 Aug 31.
9
Bidentate, monoanionic auxiliary-directed functionalization of carbon-hydrogen bonds.
Acc Chem Res. 2015 Apr 21;48(4):1053-64. doi: 10.1021/ar5004626. Epub 2015 Mar 10.
10
Copper-catalyzed enantioselective Sonogashira-type oxidative cross-coupling of unactivated C(sp)-H bonds with alkynes.
Nat Commun. 2019 Dec 12;10(1):5689. doi: 10.1038/s41467-019-13705-1.
本文引用的文献
1
Stereocontrolled synthesis of the D- and L-glycero-beta-D-manno-heptopyranosides and their 6-deoxy analogues. Synthesis of methyl alpha-l-rhamno-pyranosyl-(1-->3)-D-glycero-beta-D-manno-heptopyranosyl- (1-->3)-6-deoxy-glycero-beta-D-manno-heptopyranosyl-(1-->4)-alpha-L- rhamno-pyranoside, a tetrasaccharide subunit of the lipopolysaccharide from Plesimonas shigelloides.
J Am Chem Soc. 2006 Jun 21;128(24):8078-86. doi: 10.1021/ja061594u.
2
Benzylidene acetal fragmentation route to 6-deoxy sugars: direct reductive cleavage in the presence of ether protecting groups, permitting the efficient, highly stereocontrolled synthesis of beta-D-rhamnosides from D-mannosyl glycosyl donors. Total synthesis of alpha-D-Gal-(1-->3)-alpha-D-Rha-(1-->3)- beta-D-Rha-(1-->4)-beta-D-Glu-OMe, the repeating unit of the antigenic lipopolysaccharide from Escherichia hermannii ATCC 33650 and 33652.
J Am Chem Soc. 2004 Jul 7;126(26):8232-6. doi: 10.1021/ja048070j.
Zotero 插件