Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Zhenjie Gan"'
Autor:
Congying Pu, Yize Li, Yixian Fu, Yiyang Yan, Siyao Tao, Shuai Tang, Xiameng Gai, Ziyi Ding, Zhenjie Gan, Yingluo Liu, Siyuwei Cao, Ting Wang, Jian Ding, Jun Xu, Meiyu Geng, Min Huang
Publikováno v:
Advanced Science, Vol 11, Iss 11, Pp n/a-n/a (2024)
Abstract Intervention of the gut microbiome is a promising adjuvant strategy in cancer immunotherapy. Chemotherapeutic agents are recognized for their substantial impacts on the gut microbiome, yet their therapeutic potential as microbiome modulators
Externí odkaz:
https://doaj.org/article/3b216d8657ec4b5ebcaf0e915308894b
Publikováno v:
ACS Applied Electronic Materials. 5:1148-1155
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70eea32125bbc101dc2b81dd13248225
https://doi.org/10.1021/acsaelm.2c01617
https://doi.org/10.1021/acsaelm.2c01617
Autor:
Yameng Wan, Haixia He, Fanfan Li, Pengshuai Zhang, Xiaoqiang Gao, Yujie Wang, Zhenjie Gan, Yanxun Li
Publikováno v:
Journal of Thermal Analysis and Calorimetry. 148:2483-2499
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a26b08bbc381d034e5e5358fef63da53
https://doi.org/10.1007/s10973-022-11911-6
https://doi.org/10.1007/s10973-022-11911-6
Publikováno v:
Organic Letters. 23:3094-3099
Herein we reported a novel phosphine-catalyzed (4 + 2) cyclization reaction of electron-deficient conjugated dienes with enones to generate functionalized dihydropyran skeletons. A mechanistic investigation reveals that the reaction produces a new ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4056193bca1f22da90693f8a10ecded
https://doi.org/10.1021/acs.orglett.1c00780
https://doi.org/10.1021/acs.orglett.1c00780
Publikováno v:
Synthesis. 53:1331-1340
A highly efficient copper/GanPhos-catalyzed 1,3-dipolar cycloaddition of azomethine ylides is reported. This viable transformation provides a series of optically active spiro[dihydronaphthalene-2,3′-pyrrolidine]s, bearing one spiro quaternary a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7578f1d2e884c296e825a032778a8fc7
https://doi.org/10.1055/s-0040-1706599
https://doi.org/10.1055/s-0040-1706599
Publikováno v:
Organic Letters. 21:3210-3213
A Ag/P-stereogenic phosphine-complex-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with electron-deficient olefins is reported. In this reaction, highly functionalized pyrrolines with a spiro-quaternary stereogenic center were obtained in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4dffc7d86360e98b7dec6de7437560
https://doi.org/10.1021/acs.orglett.9b00926
https://doi.org/10.1021/acs.orglett.9b00926
Publikováno v:
Organic Letters. 21:2782-2785
A new pair of P-stereogenic ligands with multiple chiral centers were synthesized and used in the copper(I)-catalyzed enatioselective [3 + 2] cycloaddition of iminoesters with alkenes. A variety of highly functionalized pyrrolidines were obtained in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d42864a65b7f96d996c4d57c16a3894
https://doi.org/10.1021/acs.orglett.9b00734
https://doi.org/10.1021/acs.orglett.9b00734
Publikováno v:
Journal of Organometallic Chemistry. 879:158-161
P=CH2 ylides derived from ortho-alkynylphenylphosphines readily cyclize to give phosphindole derivatives. With a stabilized ylide such as P=CHC(O)Ph, the outcome of the reaction is completely different. The reaction proceeds at high temperature and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::818e2d28fcf506a3ae6e12a5973ecaca
https://doi.org/10.1016/j.jorganchem.2018.09.023
https://doi.org/10.1016/j.jorganchem.2018.09.023
Publikováno v:
Chemical Communications. 55:10120-10123
A phosphine catalyzed regiodivergent annulation of γ-substituted allenoates with conjugated dienes is reported, and highly functionalized cyclohexenes or cyclopentenes were obtained in high yields and regioselectivities. This transformation takes ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eed8ae86a8efb960f7b0de787cb95511
https://doi.org/10.1039/c9cc05207k
https://doi.org/10.1039/c9cc05207k
Publikováno v:
European Journal of Organic Chemistry. 2018:4917-4925
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62377a04a9a8d02cd70cc254d472da4c
https://doi.org/10.1002/ejoc.201800917
https://doi.org/10.1002/ejoc.201800917