Shi-Peng Luo
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Explore the profile of Shi-Peng Luo including associated specialties, affiliations and a list of published articles.
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95
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Recent Articles
1.
Gu A, Liu J, Luo S, Bi C, Su Y, Ye Z, et al.
Huan Jing Ke Xue
. 2018 Jul;
38(8):3110-3119.
PMID: 29964916
A total of 55 ambient fine particle (PM) samples were collected in Changzhou City from January to August 2016. The concentrations of 17 PM-bound PAHs in the samples were analyzed...
2.
Guo L, Huang X, Luo S, Cao W, Ruan Y, Ye J, et al.
Angew Chem Int Ed Engl
. 2016 Feb;
55(12):4064-8.
PMID: 26890255
The first total synthesis of the alkaloid (-)-haliclonin A is reported. The asymmetric synthesis relied on a novel organocatalytic asymmetric conjugate addition of nitromethane with 3-alkenyl cyclohex-2-enone to set the...
3.
Sun B, Wang Q, Yu Z, Yu Y, Xiao C, Kang C, et al.
PLoS One
. 2015 Sep;
10(9):e0137810.
PMID: 26368803
High concentrations of arsenic, which can be occasionally found in drinking water, have been recognized as a global health problem. Exposure to arsenic can disrupt spatial memory; however, the underlying...
4.
Xu C, Luo S, Wang A, Huang P
Org Biomol Chem
. 2014 Mar;
12(18):2859-63.
PMID: 24675877
We demonstrated, for the first time, that on the basis of chemistry principles, the hexacyclic peptidyl alkaloid (−)-chaetominine (1) can be synthesized in a straightforward manner from L-Trp. The approach...
5.
Peng Q, Luo S, Xia X, Liu L, Huang P
Chem Commun (Camb)
. 2014 Jan;
50(16):1986-8.
PMID: 24413776
The total synthesis of the alkaloid (-)-chaetominine (1) has been achieved in four steps with an overall yield of 33.4%. Key features of our strategy include a one-pot cascade indole...
6.
Luo S, Guo L, Gao L, Li S, Huang P
Chemistry
. 2012 Dec;
19(1):87-91.
PMID: 23225701
Three keys to success: A concise method for the construction of a tricyclic substructure (2) of haliclonin A (1) in racemic form is described (see figure). This synthesis features a...
7.
Zhou H, Liu W, Su Y, Wei Z, Liu J, Kolluri S, et al.
Cancer Cell
. 2010 Jun;
17(6):560-73.
PMID: 20541701
Nonsteroidal anti-inflammatory drugs (NSAIDs) exert their anticancer effects through cyclooxygenase-2 (COX-2)-dependent and independent mechanisms. Here, we report that Sulindac, an NSAID, induces apoptosis by binding to retinoid X receptor-alpha (RXRalpha)....