Results 201 to 210 of about 14,649 (249)
Catalytic enantioselective synthesis of inherently chiral calix[4]arenes via organocatalyzed aromatic amination enabled desymmetrization. [PDF]
Yuan M, Xie W, Yu S, Liu T, Yang X.
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Asymmetric Migratory Tsuji-Wacker Oxidation Enables the Enantioselective Synthesis of Hetero- and Isosteric Diarylmethanes. [PDF]
Frank E +7 more
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Rhodium-Catalyzed Allylic Amination for the Enantioselective Synthesis of Tertiary β-Fluoroamines. [PDF]
Chukwu FO, Arachchi MK, Nguyen HM.
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De Novo Enantioselective Synthesis of Hexafluorinated d-Glucose. [PDF]
Depienne S +4 more
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Enantioselective Synthesis of (−)-Pentalenene
Organic Letters, 2007A short, enantioselective synthesis of (-)-pentalenene is described. Catalytic enantioselective cyclopropenation with (R,R)-Rh2(OAc)(DPTI)3 was used to set the absolute stereochemistry, and an intramolecular Pauson-Khand reaction of the resulting cyclopropenyne was used to establish the quaternary center.
Joseph Fox, Joseph M Fox*
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Enantioselective Synthesis of Euonyminol
Journal of the American Chemical Society, 2021We describe an enantioselective total synthesis of the nonahydroxylated sesquiterpenoid euonyminol, the dihydro-β-agarofuran nucleus of the macrocyclic terpenoid alkaloids known as the cathedulins. Key features of the synthetic sequence include a highly diastereoselective intramolecular alkene oxyalkylation to establish the C10 quaternary center, an ...
Martin Tomanik, Zhi Xu, Seth B. Herzon
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Enantioselective Synthesis of and with Allenes.
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Anja, Hoffmann-Röder, Norbert, Krause
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Enantioselective Synthesis of (‐)‐Idiospermuline.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Larry E Overman, Emily A Peterson
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Enantioselective Synthesis of Chromenes.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Christophe Hardouin +3 more
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Enantioselective Synthesis of Renieramide.
ChemInform, 2004A highly chemo- and enantioselective PTC alkylation has been developed that allows rapid access to orthogonally protected (S,S)-isodityrosine. Utility of this material in the construction of isodityrosine-containing cyclic peptides is demonstrated by synthesis of the natural product renieramide.
Barry Lygo, Luke Humphreys
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