Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hanyang Bao"'
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
Abstract Planar chiral [2.2]paracyclophane derivatives are a type of structurally intriguing and practically useful chiral molecules, which have found a range of important applications in the field of asymmetric catalysis and material science. Howeve
Externí odkaz:
https://doaj.org/article/dc2419adf3de46bd95eb8e80464d6268
Autor:
Dekun Zhang, Ying-Bo Shao, Wansen Xie, Yunrong Chen, Wei Liu, Hanyang Bao, Faqian He, Xiao-Song Xue, Xiaoyu Yang
Publikováno v:
ACS Catalysis. 12:14609-14618
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d98fd56ff844da5a30b48584035a730e
https://doi.org/10.1021/acscatal.2c04975
https://doi.org/10.1021/acscatal.2c04975
Publikováno v:
Angewandte Chemie. 135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::392578f16bdf983a7ca404c2ff938841
https://doi.org/10.1002/ange.202300481
https://doi.org/10.1002/ange.202300481
Publikováno v:
Organic letters. 24(22)
The reactivity umpolung of the C═N bond in the quinoxaline scaffold has been successfully realized for the first time by introduction of a formyl or an acyl group adjacent to the C-position of the C═N moiety. The reversed reactivity of the C═N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78a66073b41b7f809c6691cd707a506a
https://pubmed.ncbi.nlm.nih.gov/35648469
https://pubmed.ncbi.nlm.nih.gov/35648469
Publikováno v:
ACS Catalysis. 10:7563-7572
A deoxygenative radical alkylation of aromatic alkynes with alkyl aldehydes for the preparation of allylarenes has been successfully achieved. This transformation is accomplished through the reacti...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cba24691d8af6d6a81cd29c087c2533f
https://doi.org/10.1021/acscatal.0c02454
https://doi.org/10.1021/acscatal.0c02454
Autor:
Wanmei Li, Hongdou Zhang, Jun Xu, Lin Huang, Huiyong Yang, Pengfei Zhang, Heng Cai, Hanyang Bao
Publikováno v:
Asian Journal of Organic Chemistry. 8:2105-2108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0120e9090f5982ded1a92a0f215057c
https://doi.org/10.1002/ajoc.201900548
https://doi.org/10.1002/ajoc.201900548
Publikováno v:
The Journal of Organic Chemistry. 84:3579-3589
We herein describe a B2Pin2-assisted copper-catalyzed semihydrogenation of alkynes. A variety of alkenes were obtained in good to excellent yields with Z-selectivity under mild reaction conditions. Mechanistic studies indicated that a transfer hydrog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06c946b36733c6b4a62c128f15f08f2e
https://doi.org/10.1021/acs.joc.9b00321
https://doi.org/10.1021/acs.joc.9b00321
Publikováno v:
Tetrahedron. 73:154-163
A mild and efficient protocol for the synthesis of dibenzopyranones and pyrazolobenzopyranones was developed involving a copper(0)/Selectfluor system-catalyzed double CH activation/oxygen insertion of 2-arylbenzaldehydes and 5-arylpyrazole-4-carbalde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99a791fcad88eed6863c7d47cff7a99a
https://doi.org/10.1016/j.tet.2016.11.069
https://doi.org/10.1016/j.tet.2016.11.069
Publikováno v:
Organic letters. 21(12)
The first example of oxidative C–H fluoroalkoxylation of quinoxalinones with fluoroalkyl alcohols under transition-metal and solvent-free conditions is described. This approach provides the synthesis of fluoroalkoxylated quinoxaline derivatives wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5755e905bae53058e7a73a68510ad628
https://pubmed.ncbi.nlm.nih.gov/31184162
https://pubmed.ncbi.nlm.nih.gov/31184162
Publikováno v:
Organicbiomolecular chemistry. 17(20)
An efficient and straightforward method for the synthesis of N-heteroaroyl imides has been successfully developed involving a copper-catalyzed radical-triggered three-component reaction of N-heteroaryl aldehydes, nitriles, and water. Mechanistic stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::931ef49638c4c2912dd72279091cc819
https://pubmed.ncbi.nlm.nih.gov/31044206
https://pubmed.ncbi.nlm.nih.gov/31044206