Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Xiao-Xin Shi"'
Autor:
Xing-Liang Zhu, Yong-Qiang Luo, Lei Wang, Yong-Kang Huang, Yun-Gang He, Wen-Jing Xie, Shi-Ling Liu, Xiao-Xin Shi
Publikováno v:
ACS Omega, Vol 6, Iss 26, Pp 17103-17112 (2021)
Externí odkaz:
https://doaj.org/article/5061781bcd3d4e4baaad85b42f4f1340
Autor:
Xing-Liang Zhu, Lei Wang, Yong-Qiang Luo, Yun-Gang He, Feng-Lei Li, Mian-Mian Sun, Shi-Ling Liu, Xiao-Xin Shi
Publikováno v:
ACS Omega, Vol 5, Iss 4, Pp 1813-1821 (2020)
Externí odkaz:
https://doaj.org/article/e90cc98f9afa4c04a77cbe5720ae24a3
Publikováno v:
ACS Omega, Vol 3, Iss 7, Pp 8243-8252 (2018)
Externí odkaz:
https://doaj.org/article/0e9a60b249c74e568d08eafca502ce9a
Publikováno v:
ACS Omega, Vol 3, Iss 1, Pp 544-553 (2018)
Externí odkaz:
https://doaj.org/article/486c5615aa8d48d2a549d8ea830acbb6
Publikováno v:
Synthetic Communications. 51:3427-3434
In this article, an efficient and practical stereoselective synthesis of 5a-carba-α-L-mannopyranose from naturally abundant (−)-shikimic acid is discussed. 5a-Carba-α-L-mannopyranose was synthesize...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee639c6cb9a1100d049908094dfcae28
https://doi.org/10.1080/00397911.2021.1975300
https://doi.org/10.1080/00397911.2021.1975300
Autor:
Yong-Qiang Luo, Xiao-Xin Shi, Yun-Gang He, Feng-Lei Li, Zhang-Li Xu, Wen-Jing Xie, Xing-Liang Zhu, Yong-Kang Huang
Publikováno v:
European Journal of Organic Chemistry. 2021:4318-4332
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c09a68d216c74777c8bd6992e6b3e594
https://doi.org/10.1002/ejoc.202100653
https://doi.org/10.1002/ejoc.202100653
Autor:
Yun-Gang He, Wen-Jing Xie, Shi-Ling Liu, Xiao-Xin Shi, Yong-Kang Huang, Xing-Liang Zhu, Yong-Qiang Luo, Lei Wang
Publikováno v:
ACS Omega, Vol 6, Iss 26, Pp 17103-17112 (2021)
Novel highly stereoselective syntheses of (+)-streptol and (-)-1-epi-streptol starting from naturally abundant (-)-shikimic acid were described in this article. (-)-Shikimic acid was first converted to the common key intermediate by 11 steps in 40% y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03f714b0fd0a8bf3e033d958ab2a5aac
https://doi.org/10.1021/acsomega.1c02502
https://doi.org/10.1021/acsomega.1c02502
Autor:
Bo Zheng, Qi-Qi Fan, Yong-Qiang Luo, Yun-Gang He, Xiao-Xin Shi, Yong-Kang Huang, Xing-Liang Zhu
Publikováno v:
RSC Advances. 11:29702-29710
A mild, efficient and eco-friendly method for the oxidation of 1-Bn-DHIQs to 1-Bz-DHIQs without concomitant excessive oxidation of 1-Bz-DHIQs to 1-Bz-IQs is very important for the syntheses of 1-Bz-DHIQ alkaloids and analogues. In this article, we de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd251091cb18b1d3e1e4bd1b7d3bb431
https://doi.org/10.1039/d1ra05671a
https://doi.org/10.1039/d1ra05671a
Autor:
Feng-Lei Li, Xiao-Xin Shi, Mian-Mian Sun, Lei Wang, Xing-Liang Zhu, Yun-Gang He, Shi-Ling Liu, Yong-Qiang Luo
Publikováno v:
ACS Omega, Vol 5, Iss 4, Pp 1813-1821 (2020)
ACS Omega
ACS Omega
Efficient and highly stereoselective syntheses of (+)-proto-quercitol and (-)-gala-quercitol starting from the naturally abundant (-)-shikimic acid were described in this article. (-)-Shikimic acid was first converted to the key intermediate by eight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ea6255735614c1ea4f2841652e1c35
https://doaj.org/article/e90cc98f9afa4c04a77cbe5720ae24a3
https://doaj.org/article/e90cc98f9afa4c04a77cbe5720ae24a3
Autor:
Yun-Gang, He, Yong-Kang, Huang, Qi-Qi, Fan, Bo, Zheng, Yong-Qiang, Luo, Xing-Liang, Zhu, Xiao-Xin, Shi
Publikováno v:
RSC advances. 11(47)
A mild, efficient and eco-friendly method for the oxidation of 1-Bn-DHIQs to 1-Bz-DHIQs without concomitant excessive oxidation of 1-Bz-DHIQs to 1-Bz-IQs is very important for the syntheses of 1-Bz-DHIQ alkaloids and analogues. In this article, we de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7218a77273d245868982fd6a89da61f
https://pubmed.ncbi.nlm.nih.gov/35479555
https://pubmed.ncbi.nlm.nih.gov/35479555