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Abstract Recent years have witnessed marked progress in the efficient synthesis of various enantioenriched 1,2,3,4-tetrahydroquinoxalines. However, enantio- and diastereoselective access to trans-2,3-disubstituted 1,2,3,4-tetrahydroquinoxalines remains much less explored. Herein we report that a frustrated Lewis pair-based catalyst generated via in situ hydroboration of 2-vinylnaphthalene with HB(C6F5)2 allows for the one-pot tandem cyclization/hydrosilylation of 1,2-diaminobenzenes and 1,2-diketones with commercially available PhSiH3 to exclusively afford trans-2,3-disubstituted 1,2,3,4-tetrahydroquinoxalines in high yields with excellent diastereoselectivities (>20 : 1 dr). Furthermore, this reaction can be rendered asymmetric by using an enantioenriched borane-based catalyst derived from HB(C6F5)2 and a binaphthyl-based chiral diene to give rise to enantioenriched trans-2,3-disubstituted 1,2,3,4-tetrahydroquinoxalines in high yields with almost complete diastereo- and enantiocontrol (>20 : 1 dr, up to >99 % ee). A wide substrate scope, good tolerance of diverse functionality and up to 20-gram scale production are demonstrated. The enantio- and diastereocontrol are achieved by the judicious choice of borane catalyst and hydrosilane. The catalytic pathway and the origin of the excellent stereoselectivity are elucidated by mechanistic experiments and DFT calculations. 

Wooden utility poles are one of the most commonly used utility carriers in North America. Even though they are given different protection treatments, wooden utility poles are prone to have defects that are mainly caused by temperature, oxygen, moisture, and high potential hydrogen levels after decades of being exposed in open-air areas. In order to meet the growing demand regarding their maintenance and replacement, an effective health evaluation technology for wooden utility poles is essential to ensure normal power supply and safety. However, the commonly used hole-drilling inspection method always causes extra damage to wooden utility poles and the precision of health evaluation highly relies on technician experience at present. Therefore, a non-destructive health evaluation method with frequency-modulated empirical mode decomposition (FM-EMD) and Laplace wavelet correlation filtering based on dynamic responses of wooden utility poles was proposed in this work. Specifically, FM-EMD was used to separate multiple confusing closely-spaced vibration modes due to nonlinear properties of wooden utility poles into several single modes. The instantaneous frequency and damping factor of the decomposed signal of each single mode of the dynamic response of a wooden utility pole could be determined using Laplace wavelet correlation filtering with high precision. The health status of a wooden utility pole could then be estimated according to the extracted instantaneous frequency and damping factor of the decomposed signal of each single mode. The proposed non-destructive health evaluation method for wooden utility poles was tested in the field and achieved successful results. 

A Rh( i )-catalyzed trideuteromethylation of heteroarenes with inexpensive and readily available deuterated acetic acid (CD 3 CO 2 D) with the aid of a N -containing directing groups is developed. The oxidant-free reaction is applicable to a wide range of heteroarene substrates, including 2-pyridones, indoles, aryl rings, pyrroles and carbazoles. It allows installation of CD 3 groups under straightforward reaction conditions. It is expected that the salient and practical features of this trideuteromethylation protocol will be of use to academic and industrial researchers.