Efficient C(sp3)–H Bond Functionalization of Isochroman by AZADOL Catalysis
摘要:
A novel organocatalytic C(sp(3))-H bond functionalization of isochroman under practical conditions has been developed. In the presence of 5.0 mol % of AZADOL, the catalysis proceeded successfully with a broad range of substrates and nucleophiles in excellent yields.
Structurally Diverse α-Substituted Benzopyran Synthesis through a Practical Metal-Free C(sp<sup>3</sup>)–H Functionalization
作者:Wenfang Chen、Zhiyu Xie、Hongbo Zheng、Hongxiang Lou、Lei Liu
DOI:10.1021/ol503004a
日期:2014.11.21
A trityl ion-mediated practical C–H functionalization of a variety of benzopyrans with a wide range of nucleophiles (organoboranes and C–H molecules) at ambient temperature has been disclosed. The metal-free reaction has an excellent functional group tolerance and high chemoselectivity and displays a broad scope with respect to both benzopyran and nucleophile partners, efficiently affording a collection
Simple and Direct sp<sup>3</sup> C–H Bond Arylation of Tetrahydroisoquinolines and Isochromans via 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone Oxidation under Mild Conditions
作者:Wataru Muramatsu、Kimihiro Nakano、Chao-Jun Li
DOI:10.1021/ol401534g
日期:2013.7.19
The 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)-mediated sp3C–Hbondarylation of tetrahydroisoquinolines and isochromans is described. The corresponding products were facilely synthesized via a simple nucleophilic addition reaction between readily available aryl Grignard reagents and iminium (or oxonium) cations generated in situ by DDQ oxidation of tetrahydroisoquinolines (or isochromans) under
Organocatalytic Approach for C(sp<sup>3</sup>)–H Bond Arylation, Alkylation, and Amidation of Isochromans under Facile Conditions
作者:Wataru Muramatsu、Kimihiro Nakano
DOI:10.1021/ol5006399
日期:2014.4.4
the synthesis of isochroman derivatives via direct C(sp3)–H bond arylation is described. The oxidation reaction with [bis(trifluoroacetoxy)iodo]benzene facilitates the regeneration of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in the C(sp3)–H bond arylation of isochroman. The reaction conditions can also be used for alkyl Grignard reagents and amides to afford the corresponding isochroman derivatives.
Transition-Metal-Free Cross-Coupling of Indium Organometallics with Chromene and Isochroman Acetals Mediated by BF<sub>3</sub>·OEt<sub>2</sub>
作者:José M. Gil-Negrete、José Pérez Sestelo、Luis A. Sarandeses
DOI:10.1021/acs.orglett.6b02058
日期:2016.9.2
coupling of triorganoindiumreagents with benzopyranyl acetals mediated by a Lewis acid has been developed. The reaction of R3In with chromene and isochroman acetals in the presence of BF3·OEt2 afforded 2-substituted chromenes and 1-substituted isochromans, respectively, in good yields. The reactions proceed with a variety of triorganoindiumreagents (aryl, heteroaryl, alkynyl, alkenyl, alkyl) using