Pages that link to "Q50508178"

The following pages link to Highly regioselective Lewis acid-catalyzed [3 2] cycloaddition of alkynes with donor–acceptor oxiranes by selective carbon–carbon bond cleavage of epoxides (Q50508178):

Displaying 8 items.

• [5 2] Cycloaddition of 2-(2-Aminoethyl)oxiranes with Alkynes via Epoxide Ring-Opening: A Facile Access to Azepines. (Q48143247) (← links)
• Asymmetric Synthesis of Furo[3,4-b]indoles by Catalytic [3 2] Cycloaddition of Indoles with Epoxides (Q50246783) (← links)
• An asymmetric [3 2] cycloaddition of alkynes with oxiranes by selective C-C bond cleavage of epoxides: highly efficient synthesis of chiral furan derivatives (Q50451024) (← links)
• Scandium-catalyzed tandem selective oxirane ring-opening/Friedel-Crafts alkylation: a facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines (Q50452450) (← links)
• Catalytic asymmetric [3 2] cycloaddition of aromatic aldehydes with oxiranes by C-C bond cleavage of epoxides: highly efficient synthesis of chiral 1,3-dioxolanes (Q50463652) (← links)
• C-O versus C-C bond cleavage: selectivity control in Lewis acid catalyzed chemodivergent cycloadditions of aryl oxiranyldicarboxylates with aldehydes, and theoretical rationalizations of reaction pathways. (Q50495399) (← links)
• Efficient synthesis of isochromanones and isoquinolines via Yb(OTf)3-catalyzed tandem oxirane/aziridine ring opening/Friedel-Crafts cyclization (Q50503352) (← links)
• Ni(ClO4)2-catalysed regio- and diastereoselective [3 2] cycloaddition of indoles and aryl oxiranyl-dicarboxylates/diketones: a facile access to furo[3,4-b]indoles (Q50504881) (← links)