ChemInform Abstract: Cyclization—Oxidation of 1,6-Enyne Derived from Baylis—Hillman Adducts via...

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ChemInform 2009, 40, issue 11 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Furan derivatives R 0060 Cyclization—Oxidation of 1,6-Enyne Derived from Baylis—Hillman Adducts via Pd(II)/Pd(IV)-Catalyzed Reactions: Stereoselective Synthesis of Multisubstituted Bicyclo[3.1.0]hexanes and Insight into Reaction Pathways. — In some cases, the bicyclic products are accompanied by acetates as protonolysis side products. — (LIU, H.; YU, J.; WANG, L.; TONG*, X.; Tetrahedron Lett. 49 (2008) 48, 6924-6928; Lab. Adv. Mater., Inst. Fine Chem., East China Univ. Sci. Technol., Shanghai 200237, Peop. Rep. China; Eng.) — Mais 11- 117

Transcript of ChemInform Abstract: Cyclization—Oxidation of 1,6-Enyne Derived from Baylis—Hillman Adducts via...

Page 1: ChemInform Abstract: Cyclization—Oxidation of 1,6-Enyne Derived from Baylis—Hillman Adducts via Pd(II)/Pd(IV)-Catalyzed Reactions: Stereoselective Synthesis of Multisubstituted

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Furan derivativesR 0060 Cyclization—Oxidation of 1,6-Enyne Derived from Baylis—Hillman Adducts via

Pd(II)/Pd(IV)-Catalyzed Reactions: Stereoselective Synthesis of Multisubstituted Bicyclo[3.1.0]hexanes and Insight into Reaction Pathways. — In some cases, the bicyclic products are accompanied by acetates as protonolysis side products. — (LIU, H.; YU, J.; WANG, L.; TONG*, X.; Tetrahedron Lett. 49 (2008) 48, 6924-6928; Lab. Adv. Mater., Inst. Fine Chem., East China Univ. Sci. Technol., Shanghai 200237, Peop. Rep. China; Eng.) — Mais

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ChemInform 2009, 40, issue 11 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Regioselective synthesis of multisubstituted pyrazoles via

Regioselective synthesis of multisubstituted pyrazoles via

PD-851-and-PD-626 (1)

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Stereoselective Synthesis of Multisubstituted Alkenes via

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02-1126 - Thailand - Defense · fuze, pd m739 fuze, pd m739 fuze, pd m739 fuze, pd m739 fuze, pd m739 fuze, pd m739 : 11328 2474 2474 80 2416 80 . 18852 : 17.10 3.71 3.71 0.12 3.62

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BEHAVIOR OF MULTISUBSTITUTED HYDROXYAPATITES IN …studiachemia/issues/chemia... · (ICP-OES). The results are important for the future use of these hydroxyapatite biomaterials, as

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An enyne cycloisomerization/[5+1] reaction sequence to … · 2019. 8. 7. · An enyne cycloisomerization/[5+1] r eaction sequence was developed to synthesize tetrahydroisoquinolino

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