Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Silong Xu"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract This paper addresses the challenge of low detection accuracy of grape clusters caused by scale differences, illumination changes, and occlusion in realistic and complex scenes. We propose a multi-scale feature fusion and augmentation YOLOv7
Externí odkaz:
https://doaj.org/article/6f86ed7d381240e8aa944a71dc76c389
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-9 (2023)
Abstract Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Replacement of oxoamide units with thioamides in peptide therapeutics is a valuable tactic to improve biological activity and resistance to enzy
Externí odkaz:
https://doaj.org/article/c71bbe1b8c9d43388bf3dae5b6afdffe
Autor:
Ansar Abbas, Chen Zhang, Guangwei Hu, Sameer Hussain, Ruixia Gao, Jing Li, Yang li, Silong Xu
Publikováno v:
Chemical Engineering Journal Advances, Vol 12, Iss , Pp 100394- (2022)
In the hunt of new sustainable release agents for concrete removal with improved demoulding efficacy, oil-in-dispersion (OD) release agents have appeared as favourable emulsions, since they display augmented performance in contrast to conventional oi
Externí odkaz:
https://doaj.org/article/be7e54c90cbf43b4a25e5a882f1dc79d
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 990-995 (2014)
A highly regioselective SN2' Mitsunobu reaction between Morita–Baylis–Hillman (MBH) alcohols, azodicarboxylates, and triphenylphosphine is developed, which provides an easy access to α-alkylidene-β-hydrazino acid derivatives in high yields and
Externí odkaz:
https://doaj.org/article/99eab4a88a4b446b8777d0d960ac3df1
Publikováno v:
Organic Letters. 25:2555-2559
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d86a899925c03408364bbc9552394229
https://doi.org/10.1021/acs.orglett.3c00229
https://doi.org/10.1021/acs.orglett.3c00229
Publikováno v:
The Journal of Organic Chemistry. 87:6362-6370
Herein, we describe a DABCO-catalyzed [4 + 2] annulation between 5-methylenehex-2-ynedioates and electron-deficient olefins to afford functionalized cyclohexadienes in good yields under mild conditions. The use of β- and ε-carbons of the substrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d11d511af451128c4bcaceb8ad799677
https://doi.org/10.1021/acs.joc.1c03159
https://doi.org/10.1021/acs.joc.1c03159
Autor:
Huijia Song, Feng Wang, Yayun Zhao, Ruixia Gao, Yulian He, Qing Yan, Xiaoyi Chen, Lisa D. Pfefferle, Silong Xu, Ying Sheng
Publikováno v:
Nanoscale. 14:11343-11352
As the changes of biomarkers directly reflect the occurrence of degenerative diseases, accurate detection of biomarkers is of great significance for disease diagnosis and control. However, single index detection has high uncertainties to accurately r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dabf50d1f247b9482d2e29bdec0f63f8
https://doi.org/10.1039/d2nr03356a
https://doi.org/10.1039/d2nr03356a
Publikováno v:
Organic Letters. 24:435-440
A highly efficient cascade cyclization of phenidones and enynones has been developed via a Ru(II)-catalyzed C-H activation initiated indole formation/Diels-Alder reaction/iminium ion cyclization sequence, which afforded hexacyclic indolines as single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::039e4f6a97bdb26fc9488cd1ff58ec86
https://doi.org/10.1021/acs.orglett.1c04133
https://doi.org/10.1021/acs.orglett.1c04133
Publikováno v:
Organic Letters. 23:9030-9035
Herein we describe a phosphine-catalyzed internal redox [4 + 2] annulation of 1,4-enynoates with electron-deficient alkenes, in which the γ- and φ-C(sp3)-H of the enynoates are formally oxidized for the annulation while the alkynyl moiety is conver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95e8a474699de657ac2f5a5330d20e5d
https://doi.org/10.1021/acs.orglett.1c03206
https://doi.org/10.1021/acs.orglett.1c03206
Publikováno v:
Organic Letters. 23:8365-8369
A rhodium-catalyzed diastereoselective formal [5 + 2] annulation of indoles with cyclohexadienone-containing 1,6-enynes has been established via indole 2,3-difunctionalization. The reaction, probably proceeding through tandem indole C2-H alkenylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73d25b11485a2d84f6567e50ae95f6a1
https://doi.org/10.1021/acs.orglett.1c03106
https://doi.org/10.1021/acs.orglett.1c03106