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| 1 | Visible Light Promoted β-C-H Alkylation of β-Ketocarbonyls via a β-Enaminyl Radical Intermediate显示文摘 | Dehong Wang Long Zhang Sanzhong Luo | 2018 | Chinese Journal of Chemistry2018，36，4： | 4 |
| 2 | Functionalized ionic liquids catalyzed direct aldol reactions 显示文摘 | Luo Sanzhong Mi Xueling Zhang Long | 2007 | Tetrahedron2007，63，： | 1 |
| 3 | Functionalized ionic liquids catalyzed direct aldol reactions 显示文摘 | Luo Sanzhong Mi Xueling Zhang Long | 2007 | Tetrahedron2007，63，： | 1 |
| 4 | Recent progress in lantha-nide-catalyzed organic reactions in protic media显示文摘Lanthanide triflates are stable in water. It is possible for lanthanides to undergo many organic reactions in environmentally friendly solvents. This makes lanthanides very promising in the field of green chemistry. This review describes the recent development of the lanthanide-catalyzed organic reactions in protic solvents. Those reac-tions include Diels-Alder, Aldol, Allylation, acetalization, pericyclization, radical reactions as well as some newly-developed lanthnides-based catalysts. | LUO Sanzhong ZHANG Baolian XIAN Ming Adam Janczuk XIE Wenhua CHENG Jinpei Peng George Wang | 2001 | Chinese Science Bulletin2001，46，20： | 1 |
| 5 | Asymmetric α-Alkylation of β-Ketocarbonyls via Direct Phenacyl Bromide Photolysis by Chiral Primary Amine显示文摘 | Wenzhao Zhang Yunbo Zhu Long Zhang Sanzhong Luo | 2018 | Chinese Journal of Chemistry2018，36，8： | 1 |
| 6 | Chiral amine- polyoxometalate hybrids as highly efficient and recoverable asymmetric enamine catalysts 显示文摘 | Luo Sanzhong Li Jiuyuan Xu Hui | 2007 | Org Lett2007，9，18： | 1 |
| 7 | Interactions between SIRT1 and MAPK/ERK regulate neuronal apoptosis induced by traumatic brain injury in vitro and in vivo显示文摘 | Yongbo Zhao Peng Luo Qindong Guo Sanzhong Li Lei Zhang Mingming Zhao Haoxiang Xu Yuefan Yang Waisang Poon Zhou Fei | 2012 | Experimental Neurology2012，，2： | 1 |
| 8 | Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes显示文摘Simple pyrrolidine-azole conjugates have been synthesized and found to be efficient catalysts for asymmetric Michael addition to nitrostyrenes. The identified optimal catalysts, pyrrolidine-azoles 2, 8 and 13, could catalyze the asymmetric Michael addition of a range of Michael donors and nitrostyrenes in high yields (up to 99%) and excellent stereoselectivities (up to 99:1 dr and 97% ee). | ZHANG Long XU Hui MI XueLing LUO SanZhong CHENG Jin-Pei | 2010 | Chinese Science Bulletin2010，55，17： | 1 |
| 9 | LA-ICP-MS U-Pb Zircon Geochronology of the Yushulazi Group in the Eastern Block, North China Craton显示文摘 | Yan Luo Min Sun Guochun Zhao Sanzhong Li Xiaoping Xia | 2006 | International Geology Review2006，，9： | 1 |
| 10 | Bifunctional catalysis of Morita-Baylis-Hillman (MBH) reaction with chiral primary-tertiary diamine: A non-typical MBH catalytic pathway显示文摘A simple primary-tertiary diamine has been explored as a novel catalyst for the Morita-Baylis-Hillman reaction of MVK and aryl aldehydes, and moderate to good chemical yields were obtained. Detailed mechanism study indicated that the diamine acted as a bifunctional cooperation catalyst via a bicyclic enamino-quaternary ammonium intermediate. | ZHANG Long LUO SanZhong CHEN LiuJuan LI JiuYuan CHENG JinPei | 2009 | Science China Chemistry2009，52，9： | 0 |
| 11 | Biomimetic asymmetric catalysis显示文摘Enzymes are the core for biological transformations in nature.Their structures and functions have drawn enormous attention from biologists as well as chemists since last century.The large demand of bioactive molecules and the pursuit of efficiency and greenness of synthesis have spurred the rapid development of biomimetic chemistry in the past several decades.Biomimetic asymmetric catalysis,mimicking the structures and functions of enzymes,has been recognized as one of the most promising synthetic strategies for the synthesis of valuable chiral compounds.This review summarizes the evolution of asymmetric catalysis inspired by aldolases,vitamin B_(1)/B_(6)-dependent enzymes,NAD(P)H,flavin,hydrogenases,heme oxygenases,nonheme oxygenases,and dinuclear/multinuclear metalloenzymes in aspects of biomimetic design,catalyst development and related catalytic transformations.Those well-established synthetic approaches originating from biological reactions have demonstrated the unique prowess of biomimetic asymmetric catalysis in bridging the gap between bio-catalysis and chemical synthesis. | Xiao Xiao Kaini Xu Zhong-Hua Gao Zhou-Hao Zhu Changqing Ye Baoguo Zhao Sanzhong Luo Song Ye Yong-Gui Zhou Senmiao Xu Shou-Fei Zhu Hongli Bao Wei Sun Xiaoming Wang Kuiling Ding | 2023 | Science China Chemistry2023，66，6： | 0 |
| 12 | Primary-Tertiary Diamine/Brønsted Acid Catalyzed α-Allylation of Carbonyl Compounds with Allylic Alcohols显示文摘A simple and directα-allylic alkylation of unmodified aldehydes with allylic alcohols catalyzed by primary amine/Brønsted acid has been developed.The N,N-dimethylethylenediamine/TfOH was identified as the optimal catalyst to promote this transformation via an enamine process in high yields(up to 88%)and with good diastereoselectivities(up to 9∶1). | Lingyun Cui Long Zhang Sanzhong Luo Jin-Pei Cheng | 2014 | Chinese Journal of Chemistry2014，32，8： | 0 |
| 13 | Visible Light Promoted Direct Deuteration of Alkenes via Co(III)–H Mediated H/D Exchange显示文摘We report herein a visible light-mediated direct deuteration of alkenes with D_(2)O or deuterated methanol(MeOD)using a cobaloxime as a hydrogen/deuterium(H/D)exchange catalyst.The synergistic photoredox/Co catalysis enabled facile deuterium(D)-incorporation of a variety of terminal and internal alkenes at either terminal or benzylic positions.We proposed that this process proceeded through a sequence of reversible addition-elimination reactions and fast proton exchange involving Co(III)–H,which was generated in situ by photoreduction. | Zongbin Jia Sanzhong Luo | 2023 | CCS Chemistry2023，5，5： | 0 |
| 14 | Bio-inspired quinone catalysis显示文摘Quinoproteins are an important type of redox enzymes for biological oxidation processes. Inspired by the quinone cofactors, particularly from copper amine oxidases, a number of small molecular quinone catalysts have been developed for C-H functionalizations of amines. Bio-inspired quinone catalysts have significantly expanded the substrate scope to include branched primary amines, secondary amines and tertiary amines, far beyond the scope of quinoproteins. This review summarizes the evolution of quinone catalysts, their mechanism and catalytic applications. | Ruipu Zhang Sanzhong Luo | 2018 | Chinese Chemical Letters2018，29，8： | 0 |
| 15 | Asymmetric α-Pentadienylation of β-Ketocarbonyls and Aldehydes by Synergistic Pd/Chiral Primary Amine Catalysis显示文摘Direct alkylation with skipped enynes or cyclopropropylacetylenes represents an ideal process for the installation of pentadienyl group in terms of atom- and step-economy.The development of catalytic asymmetric versions has been frequently pursued and most of the successes have been achieved with enolizable aldehydes.We herein describe a synergistic chiral primary amine/Pd catalysis for asymmetric α-pentadienylation of β-ketocarbonyls and aldehydes with skipped enynes or cyclopropropylacetylenes.The reaction features the construction of acyclic all-carbon quaternary centers with high enantioselectivity,and good functional group tolerance and scalability. | Chang You Sanzhong Luo | 2023 | Chinese Journal of Chemistry2023，41，24： | 0 |
| 16 | Catalytic asymmetric oxidative sulfenylation of β-ketocarbonyls using a chiral primary amine显示文摘Enantioselective oxidative construction of a C(sp^(3))–S bond has been achieved using a chiral primary amine catalyst in the presence of tert-butyl hydroperoxide and a catalytic amount of tetrabutylammonium iodide.The distinctive feature of the current reaction is coupling with nucleophilic sulfur reactants under oxidative conditions.This protocol provides facile access to chiral thioethers bearing S-containing quaternary stereocenters with good chemo-and enantiocontrol. | Qi Zhang Mingying Shi Xueling Mi Sanzhong Luo | 2022 | Organic Chemistry Frontiers2022，9，5： | 0 |
| 17 | Bio-inspired Small Molecular Catalysis显示文摘What is the most favorite and original chemistry developed in your researchgroup?I hope it's always the next one.How do you get into this specific field?Could you please share some experiences with ourreaders?Nature provides many astonishing catalytic machineries for building up molecular complexity and harnessing energy in the most efficient ways.Nature's recipe for catalysis serves as a starting point to develop new catalyst for synthetic and energy chemistry. | Mao Cai Runze Zhang Chunming Yang Sanzhong Luo | 2023 | Chinese Journal of Chemistry2023，41，5： | 0 |
| 18 | Understanding how charge-charge interaction affects the stereochemistry of enamine fluorination by chiral primary amine catalysis显示文摘Electrostatic interaction, especially electrostatic attraction, usually plays critical roles in controlling the reactivity and selectivity in catalytic transformations;however, the like-charge repulsion, which is ubiquitous in physical systems, is rarely applied in reaction control. Herein we disclosed an unexpected like-charge repulsion induced enantio-control mode in primary aminecatalyzed fluorination reactions with 1-fluoro-2,4,6-trimethylpyridinium triflate. The ionic reaction works favorably in both highly polar(methanol) and non-polar(hexane) solvents, a seldom observed phenomenon in asymmetric catalysis. Erying plot analysis showed that an inversion temperature existed in Me OH, which was explained by the solvent-solute cluster model under different temperatures. Density functional theory(DFT) study and energy decomposition analysis(EDA) verified that the likecharge repulsion takes effect in polar solvent methanol, while in nonpolar solvents, the steric repulsion associated with ion-pair was found to be the major effect for the observed enantioselectivity. | Yanfang Han Kai Yang Long Zhang Sanzhong Luo Jin-Pei Cheng | 2023 | Science China Chemistry2023，66，10： | 0 |
| 19 | Catalytic Asymmetric Addition and Telomerization of Butadiene with Enamine Intermediates显示文摘Herein,we report tunable asymmetric addition and telomerization of butadiene by synergistic chiral primary amine/achiral palladium catalysis.A selection of different achiral phosphine ligand in concert with the chiral primary amine-trifluoromethanesulfonic acid(TfOH)conjugates enables both chemo-and enantioselective control of the coupling with butadiene.Bidentate[(oxydi-2,1-phenylene)-bis-(diphenylphosphine)](DPEPhos)ligand led to 1,4-addition adduct whereas monodentate(p-Tol)3P ligand gave the telomerization product.A range ofα-branchedβ-ketoesters and aldehydes could be applied to afford allylation or telomerization products bearing allcarbon quaternary centers at high efficiency and good chemo-,regio-,and stereoselectivities. | Yaning Wang Jie Zhang Chang You Xueling Mi Sanzhong Luo | 2022 | CCS Chemistry2022，4，7： | 0 |
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