Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Wan-Wan Yang"'
Autor:
Yi Huang, Xiao-Xia Wang, Dong-Dong Sun, Ze-Xin Zhang, Wan-Wan Yang, Tian Shao, Han Han, Er-Fei Zhang, Zhong-Shu Pu, Zuo-Xu Hou, Hai-Long Dong, Li-Ze Xiong, Li-Chao Hou
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 7, Pp 840-853 (2017)
Background: Sepsis is a major cause of mortality in Intensive Care Units. Anesthetic dose isoflurane and 100% oxygen were proved to be beneficial in sepsis; however, their application in septic patients is limited because long-term hyperoxia may indu
Externí odkaz:
https://doaj.org/article/77f53972ede346c49137c18353418fec
Publikováno v:
The Journal of Organic Chemistry. 88:3079-3088
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ba529e5578a8b7e24b19a10818f9152
https://doi.org/10.1021/acs.joc.2c02870
https://doi.org/10.1021/acs.joc.2c02870
Publikováno v:
The Journal of organic chemistry. 87(18)
A facile and efficient base-mediated divergent annulation of methyl 2-(cyanomethyl)benzoates and conjugated ynones has been described. A broad range of 1-naphthols and xanthones were formed in moderate to excellent yields. The notable features of thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91458cb51a416aadef4dc0e56a5776e4
https://pubmed.ncbi.nlm.nih.gov/36062305
https://pubmed.ncbi.nlm.nih.gov/36062305
Publikováno v:
The Journal of Organic Chemistry. 86:169-177
A simple and effective annulation of ynediones and (iso)quinoline N-oxides was developed to afford various functionalized pyrrolo[2,1-a]isoquinolines and pyrrolo[1,2-a]quinolines in moderate to excellent yields. This protocol underwent a tandem [3 +
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9aa7be578bdddbaf860a5f705211071
https://doi.org/10.1021/acs.joc.0c01932
https://doi.org/10.1021/acs.joc.0c01932
Publikováno v:
Chemical Communications. 56:1183-1186
An effective annulation of ynones and (iso)quinoline N-oxides was developed to deliver various functionalized 3-((iso)quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino[2,1-a]quinolin-13-ones in moderate to excellent yields, respectively. This pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ba100b7a58ea79aa476a97e951c262
https://doi.org/10.1039/c9cc08713c
https://doi.org/10.1039/c9cc08713c
Publikováno v:
The Journal of organic chemistry. 86(21)
A simple and effective tandem reaction of diynones and allylic alcohols was developed to afford functionalized 3-allyl-4-pyrones in moderate to excellent yields. This protocol underwent a Michael addition─Claisen rearrangement─O-cyclization proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ace42776f750fc7f228caab94095356
https://pubmed.ncbi.nlm.nih.gov/34658239
https://pubmed.ncbi.nlm.nih.gov/34658239
Autor:
Lu-Lu Chen, Jing-Wen Zhang, Jun-Yan Zhu, Wan-Wan Yang, Ji-Ya Fu, Yan-Bo Wang, Pei Chen, Shuai Zhang
Publikováno v:
Organic Letters. 21:5457-5461
An effective base-controlled divergent annulation reaction of 2-bromophenylacetonitriles and ynones has been developed. Various functionalized 5-cyanobenzoxepines and benzofuro[2,3-b]pyridines were obtained with a broad substrate scope and high regio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bb62e13528bc7981fc24bc8f06bda9b
https://doi.org/10.1021/acs.orglett.9b01700
https://doi.org/10.1021/acs.orglett.9b01700
Publikováno v:
The Journal of Organic Chemistry. 84:8090-8099
Effective transition-metal-free formal [4+2] benzannulation for the preparation of 1-cyano-3-acylnaphthalenes from 2-(2-alkynylphenyl)acetonitriles and alkynones through sequential C-C bond coupling has been developed. This protocol is characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe53cdd2085cbcad1c143613f9a3b12c
https://doi.org/10.1021/acs.joc.9b00948
https://doi.org/10.1021/acs.joc.9b00948
Publikováno v:
Organic & Biomolecular Chemistry. 17:7461-7467
An effective transition-metal-free strategy was developed for the preparation of chromones from o-bromoaryl ynones and benzaldehyde oxime through sequential C-O bond formation. This cyclization reaction could well tolerate a wide range of functional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15b0611e2a4c1b4b2437be14eae4f791
https://doi.org/10.1039/c9ob01387c
https://doi.org/10.1039/c9ob01387c
Publikováno v:
The Journal of organic chemistry. 86(1)
A simple and effective annulation of ynediones and (iso)quinoline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51c842c90b9bc140a3f1c0fe9b974aab
https://pubmed.ncbi.nlm.nih.gov/33252226
https://pubmed.ncbi.nlm.nih.gov/33252226