Zobrazeno 1 - 10
of 196
pro vyhledávání: '"Honggen, Wang"'
Autor:
Jun-Yunzi Wu, Long-Ling Huang, Jia-Luo Fu, Jia-Yi Li, Shuang Lin, Shuang Yang, Zhi-Shu Huang, Honggen Wang, Qingjiang Li
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-8 (2024)
Abstract Both the pyrroloindoline core and N–CF3 moiety hold significant importance in medicinal chemistry. However, to date, no instances of constructing N–CF3-containing pyrroloindolines have been reported. Herein, we present a robust and opera
Externí odkaz:
https://doaj.org/article/c2f779f2c1d84c99a1b19e35f7edd985
Autor:
Shijia Li, Weini Li, Naseeb Kaur Malhi, Junwei Huang, Quanqi Li, Ziwei Zhou, Ruiheng Wang, Jiangling Peng, Tong Yin, Honggen Wang
Publikováno v:
Molecules, Vol 29, Iss 22, p 5471 (2024)
Cannabigerol (CBG), a non-psychoactive cannabinoid found in cannabis, has emerged as a promising therapeutic agent with a diverse range of potential applications. Unlike its well-known counterpart tetrahydrocannabinol (THC), CBG does not induce intox
Externí odkaz:
https://doaj.org/article/b40c8e91ea9445f3bdbdfb7f41f6f91e
Publikováno v:
Advanced Science, Vol 11, Iss 21, Pp n/a-n/a (2024)
Abstract The synthesis of allenyl boronates is an important yet challenging topic in organic synthesis. Reported herein is an NHC‐gold‐catalyzed 1,3‐H shift toward allenyl boronates synthesis from simple propargylic B(MIDA)s. Mechanistic studie
Externí odkaz:
https://doaj.org/article/f7dba9e03f834b3ba99b0ed130b29b11
Publikováno v:
Tetrahedron Chem, Vol 8, Iss , Pp 100052- (2023)
Indolines, characterized by their diverse biological activities and structural significance, have garnered considerable attention in the realms of natural product synthesis and drug discovery. Concurrently, the incorporation of fluorine atoms into or
Externí odkaz:
https://doaj.org/article/5415812f583c4202a09f113b33a4a75b
Autor:
Yin Li, Zhi‐Hao Chen, Shuang Lin, Yuan Liu, Jiasheng Qian, Qingjiang Li, Zhi‐Shu Huang, Honggen Wang
Publikováno v:
Advanced Science, Vol 10, Iss 30, Pp n/a-n/a (2023)
Abstract Electrophilic addition reaction to alkynes is of fundamental importance in organic chemistry, yet the regiocontrol when reacting with unsymmetrical 1,2‐dialkyl substituted alkynes is often problematic. Herein, it is demonstrated that the r
Externí odkaz:
https://doaj.org/article/77a492a0b79d45a38ffcbbada6fbb9e4
Publikováno v:
iScience, Vol 26, Iss 3, Pp 106255- (2023)
Summary: The primary amino group has been seldom utilized as a transformable functionality in organic synthesis. Reported herein is a deaminative halogenation of primary amines using N-anomeric amide as the nitrogen-deletion reagent. Both aliphatic a
Externí odkaz:
https://doaj.org/article/323331a7be00425fb4c6897daca32e75
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Alkyl carboxylic acids and primary amines are ubiquitous and useful for synthesis of new compounds. Here, the authors report a manganese-mediated reductive decarboxylative/deaminative functionalization of activated aliphatic acids and primary amines
Externí odkaz:
https://doaj.org/article/89f05c7d9acb4c02bc6f16d5f62bae88
Publikováno v:
ACS Catalysis. 13:5096-5103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b02e7318c75a718011bf215a06c6c1a1
https://doi.org/10.1021/acscatal.3c00305
https://doi.org/10.1021/acscatal.3c00305
Autor:
Yin Li, Wen-Xin Fan, Shuang Luo, Alina Trofimova, Yuan Liu, Jiang-Hao Xue, Ling Yang, Qingjiang Li, Honggen Wang, Andrei K. Yudin
Publikováno v:
Journal of the American Chemical Society. 145:7548-7558
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce58ce93749200d720fcfa545a9857a1
https://doi.org/10.1021/jacs.3c00860
https://doi.org/10.1021/jacs.3c00860
Publikováno v:
Organic Letters. 25:1099-1103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac0f99af18b689b3361d196ddf7848bc
https://doi.org/10.1021/acs.orglett.2c04343
https://doi.org/10.1021/acs.orglett.2c04343