Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jie-Min Luo"'
Publikováno v:
Clinical and Experimental Pharmacology and Physiology. 48:831-836
Objective To investigate the clinical features, treatment and prognosis of critical illness polyneuromyopathy (CIPNM) in patients with severe traumatic brain injury (sTBI) who had positive anti-ganglioside GM1 (anti-GM1) antibody IgG. Methods a case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44f7732503787f367af2c35e9bf69148
https://doi.org/10.1111/1440-1681.13496
https://doi.org/10.1111/1440-1681.13496
Publikováno v:
Brain injury. 31(5)
The study aims to explore the effects of different levels of haemoglobin (Hb) on early cerebral metabolism in patients with postoperative severe traumatic brain injury (TBI) .Fifty-nine patients were randomly divided into catheter oxygen group and ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28709831ee4aa6e2bc50aee61929ea3a
https://pubmed.ncbi.nlm.nih.gov/28350181
https://pubmed.ncbi.nlm.nih.gov/28350181
Publikováno v:
Chemistry - A European Journal. 19:13075-13086
Amides are a class of highly stable and readily available compounds. The amide functional group constitutes a class of powerful directing/activating and protecting group for C-C bond formation. Tertiary tert-alkylamine, including 1-azaspirocycle is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60248e1a7a3fb505158d927ad6c71107
https://doi.org/10.1002/chem.201302096
https://doi.org/10.1002/chem.201302096
Publikováno v:
Angewandte Chemie. 122:3101-3104
NSF of China [20832005]; National Basic Research Program (973 Program) of China [2010CB833200]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::087015cda90186ef26c1316853b1d88c
https://doi.org/10.1002/ange.201000652
https://doi.org/10.1002/ange.201000652
Publikováno v:
Chemistry - An Asian Journal. 4:328-335
Guided by nature: A flexible and epimerization-free approach for the asymmetric syntheses of melleumin A and four analogues of melleumins A and B was developed, which allowed confirming the stereochemistry at C-4 of melleumin A, and revealed that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb28560f6c2a4f4fc705bb5c958f9dd6
https://doi.org/10.1002/asia.200800355
https://doi.org/10.1002/asia.200800355
Publikováno v:
ChemInform. 45
Amides are a class of highly stable and readily available compounds. The amide functional group constitutes a class of powerful directing/activating and protecting group for C-C bond formation. Tertiary tert-alkylamine, including 1-azaspirocycle is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9c98e5985186d17e12125d87eb8432c
https://doi.org/10.1002/chin.201409106
https://doi.org/10.1002/chin.201409106
Publikováno v:
ChemInform. 43
Coupling of the furan (I) with the imines (R)- and (S)-(II) allows a stereoselective access to butenolides like (III).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11b8130cc6a4639019b1146bb0749951
https://doi.org/10.1002/chin.201203079
https://doi.org/10.1002/chin.201203079
Publikováno v:
Organic letters. 13(18)
Asymmetric vinylogous Mannich reaction (VMR) of 2-(tert-butyldimethylsilyloxy)furan (TBSOF, 1) with (R(S))- or (S(S))-t-BS-imines (3) furnished 5-aminoalkylbutenolides 7a-k in 75-87% yields with anti/syn ratios ranging from 75:25 to 97:3. Butenolides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c9fc39c3f9e0d8cf1ba4cc3d1b4ab42
https://pubmed.ncbi.nlm.nih.gov/21854016
https://pubmed.ncbi.nlm.nih.gov/21854016
Publikováno v:
ChemInform. 41
The title reaction provides a highly efficient and general method to prepare cyclic and acyclic tertiary amines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9ca0ea71786fd88598232833cc00ff1
https://doi.org/10.1002/chin.201032065
https://doi.org/10.1002/chin.201032065
Publikováno v:
Organic Letters; Sep2011, Vol. 13 Issue 18, p4938-4941, 4p