Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Man-Yi Han"'
Publikováno v:
Molecules, Vol 28, Iss 15, p 5685 (2023)
A novel double Friedel–Crafts reaction of acylsilanes in water is described. This strategy enables synthesis of bis(indolyl)methane derivatives with 1-hydroxy or 1-silyl substituents in moderate to high yield. Compared to the 1-silyl-bis(indolyl)me
Externí odkaz:
https://doaj.org/article/4e6b9811f42c4fc8b60a76e4c5ed446d
Publikováno v:
Advanced Synthesis & Catalysis. 363:2670-2675
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddcc60f775c7d87aa748d741f6b14430
https://doi.org/10.1002/adsc.202100106
https://doi.org/10.1002/adsc.202100106
Autor:
Zhiming Wang, Xiaofei Xie, Yongmin Ma, Hong Pan, Jianguo Yang, Tai-Ping Zhou, Man-Yi Han, Rong-Zhen Liao, Xiao Geng, Lei Wang, Pinhua Li
Publikováno v:
Organic Chemistry Frontiers. 8:5872-5887
A highly regioselective and diastereoselective [2 + 2] cross-photocycloaddition between electron-poor and electron-rich/electron-neutral alkenes under visible-light irradiation was developed. In the absence of an external photocatalyst, additive and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5251c13c455e0285f049bc65c1a403e6
https://doi.org/10.1039/d1qo01017d
https://doi.org/10.1039/d1qo01017d
Publikováno v:
Organic Letters. 23:54-59
A novel hydrogen-bond-assisted sequential reaction of silyl glyoxylates is described. This method provides an efficient strategy for the synthesis of silyl enol ethers with high selectivity. In these transformations, hydrogen bonds from 2-nitroethano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d21cc8eff3c1b441e5a0ccd5618a784
https://doi.org/10.1021/acs.orglett.0c03683
https://doi.org/10.1021/acs.orglett.0c03683
Publikováno v:
The Journal of Organic Chemistry. 85:5825-5837
An efficient Prins reaction of silyl glyoxylates in the presence of an aqueous ZnCl2 complex as a catalyst was developed, providing functionalized tertiary α-silyl alcohols in high yields under mil...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ed74a8aa201c8a3300bff18b629f1ad
https://doi.org/10.1021/acs.joc.9b03501
https://doi.org/10.1021/acs.joc.9b03501
Publikováno v:
Organic & Biomolecular Chemistry. 17:6612-6619
A visible-light-induced deboronative alkylarylation of acrylamides with organoboronic acids was developed. In this transformation, boronic acids could be activated by the organic photocatalyst of eosin Y, generating alky free radicals in high efficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0fb9a8af06d9a71782a0de6f5197aab
https://doi.org/10.1039/c9ob01023h
https://doi.org/10.1039/c9ob01023h
Autor:
Xiaofei Xie, Yongmin Ma, Zhiming Wang, Tai-Ping Zhou, Rong-Zhen Liao, Hong Pan, Xiao Geng, Lei Wang, Pinhua Li, Jianguo Yang, Man-Yi Han
A highly regioselective and diastereoselective [2+2] cross-photocycloaddition between the electron-poor and electron-rich/electron-neutral alkenes under visible-light irradiation was developed. In the absence of an external photocatalyst, the substra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b0ab2beca27b15a03224321915bd6af
https://doi.org/10.21203/rs.3.rs-523200/v1
https://doi.org/10.21203/rs.3.rs-523200/v1
Publikováno v:
The Journal of organic chemistry. 85(9)
An efficient Prins reaction of silyl glyoxylates in the presence of an aqueous ZnCl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ae3fa69a01d401c64eaa6dfee4ca897
https://pubmed.ncbi.nlm.nih.gov/32250619
https://pubmed.ncbi.nlm.nih.gov/32250619
Publikováno v:
European Journal of Organic Chemistry. 2018:5954-5960
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b69db770788c9b5811828b3b26cd1817
https://doi.org/10.1002/ejoc.201800963
https://doi.org/10.1002/ejoc.201800963
Publikováno v:
Organic & Biomolecular Chemistry. 16:4117-4126
A catalyst-controlled switchable reaction of β-keto acids to silyl glyoxylates was developed under mild conditions, providing two distinct products in good yields. Compared to decarboxylative addition-Brook rearrangement, the decarboxylative additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f713c261c0fbd8ce3274020e1c32cc17
https://doi.org/10.1039/c8ob00740c
https://doi.org/10.1039/c8ob00740c