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上海药物研究所 [4]

大连化学物理研究所 [4]

兰州大学 [3]

上海有机化学研究所 [3]

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	Palladium-Catalyzed Propargylic [n+2] Cycloaddition: An Efficient Strategy for Construction of Benzo-Fused Medium-Sized Heterocycles 期刊论文 ADVANCED SYNTHESIS & CATALYSIS, 2019, 卷号: 361, 期号: 4, 页码: 836-841 作者: Liu, Zhen-Ting; Hu, Xiang-Ping 收藏 \| 浏览/下载：52/0 \| 提交时间：2019/06/20 A regioselective palladium-catalyzed formal [n+2] cycloaddition of propargylic esters as C-2-synthons with various linker-tethered bisphenols for the construction of medium-sized heterocycles bearing an exocyclic double bond has been developed The reaction features mild conditions and broad substrate scopes as well as readily available substrates and catalysts Under optimal conditions various medium-sized heterocycles from eight to eleven-membered rings can be afforded in good to excellent yields and regioselectivities with high Z-selectivity for the exocyclic double bond palladium medium-sized ring propargylic ester bisphenol cycloaddition
	Palladium-catalyzed propargylic [n+2] cycloaddition: an efficient strategy for construction of benzo-fused medium-sized heterocycles 期刊论文 Advanced synthesis & catalysis, 2019, 卷号: 361, 期号: 4, 页码: 836-841 作者: Liu, Zhen-Ting; Hu, Xiang-Ping 收藏 \| 浏览/下载：78/0 \| 提交时间：2019/05/08 A regioselective palladium-catalyzed formal [n+2] cycloaddition of propargylic esters as c-2-synthons with various linker-tethered bisphenols for the construction of medium-sized heterocycles bearing an exocyclic double bond has been developed The reaction features mild conditions and broad substrate scopes As well as readily available substrates and catalysts Under optimal conditions Various medium-sized heterocycles from eight to eleven-membered rings can be afforded in good to excellent yields and regioselectivities with high z-selectivity for the exocyclic double bond Palladium Medium-sized ring Propargylic ester Bisphenol Cycloaddition
	NHPI- and TBAI-Co-Catalyzed Synthesis of Allylic Esters from Toluene Derivatives and Alkenes 期刊论文 SYNLETT, 2018, 卷号: 29, 页码: 840-844 作者: Li, Chengliang[1]; Deng, Hongmei[2]; Jin, Tao[3]; Li, Chunju[4]; Jia, Xueshun[5] 收藏 \| 浏览/下载：6/0 \| 提交时间：2019/04/24 oxyacylation toluene derivatives oxidative coupling allylic ester metal-free
	Synergistic Cu/Pd Catalysis for Enantioselective Allylation of Ketimine Esters: The Direct Synthesis of alpha-Substituted alpha-Amino Acids and 2H-Pyrrols 期刊论文 ADVANCED SYNTHESIS & CATALYSIS, 2018, 卷号: 360, 期号: 24 作者: Wei, Liang; Xiao, Lu; Wang, Chun-Jiang 收藏 \| 浏览/下载：6/0 \| 提交时间：2019/12/05 synergistic catalysis allylic alkylation ketimine ester nonproteinogenic alpha-amino acids
	钴催化烯丙基C(sp3)-H键氧化酯化机理研究及β-大马烯酮合成工艺优化学位论文 : 中国科学院大学, 2017 作者: 任天鹭收藏 \| 浏览/下载：27/0 \| 提交时间：2019/04/02 Β-大马烯酮,Co(Ii)催化,c(Sp3)-h键活化,氧化酯化,自由基反应
	Chiral phosphine-phosphoramidite ligands in asymmetric catalysis 期刊论文 SYNTHETIC COMMUNICATIONS, 2016, 卷号: 46, 期号: 11, 页码: 917-941 作者: Chen, Xiu-Shuai; Hou, Chuan-Jin; Hu, Xiang-Ping 收藏 \| 浏览/下载：16/0 \| 提交时间：2019/06/20 Asymmetric Catalysis Chiral Ligand Hydroformylation Hydrogenation Phosphine-phosphoramidite
	Recent Developments in Pd-Catalyzed Oxidative Heck Cross Coupling Reaction of Arenes/Alkenes with Allylic Esters 期刊论文 CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2015, 卷号: 35, 期号: 3, 页码: 522-527 作者: Shang, XJ; Liu, ZQ 收藏 \| 浏览/下载：3/0 \| 提交时间：2017/01/11 Pd-catalysis oxidative Heck reaction allylic ester C-H activation C-C bond formation
	Vegetable-oil-based polymers as future polymeric biomaterials 期刊论文 ACTA BIOMATERIALIA, 2014, 卷号: 10, 期号: 4, 页码: 1692-1704 作者: Miao, Shida; Wang, Ping; Su, Zhiguo; Zhang, Songping 收藏 \| 浏览/下载：27/0 \| 提交时间：2014/08/28 Vegetable-oil Biomaterial Polyurethane Polyester Polyether
	Oxidative stability and cold flow behavior of palm, sacha-inchi, jatropha and castor oil biodiesel blends 期刊论文 Fuel Processing Technology, 2012, 卷号: 102, 页码: 96-101 Zuleta, E. C. 收藏 \| 浏览/下载：7/0 \| 提交时间：2015/01/28
	Oxidative stability and cold flow behavior of palm, sacha-inchi, jatropha and castor oil biodiesel blends 期刊论文 Fuel Processing Technology, 2012, 卷号: 102, 页码: 96-101 Zuleta, E. C. 收藏 \| 浏览/下载：13/0 \| 提交时间：2015/02/11

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