Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles

Publisher： John Wiley & Sons Inc

E-ISSN： 1521-3773|54|18|5460-5464

ISSN： 1433-7851

Source： ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol.54, Iss.18, 2015-04, pp. : 5460-5464

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles

By  

ANGEWANDTE CHEMIE, Vol. 127, Iss. 18, 2015-04 ,pp. : 5550-5554

John Wiley & Sons Inc

Access to resources Recommend Favorite

Stereoselective Synthesis of Hydropyrano[3,2‐b]indoles via Organocatalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction

By  

ADVANCED SYNTHESIS & CATALYSIS, Vol. 358, Iss. 18, 2016-09 ,pp. : 2970-2975

John Wiley & Sons Inc

Access to resources Recommend Favorite

Front Cover Picture: Stereoselective Synthesis of Hydropyrano[3,2‐b]indoles via Organocatalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction (Adv. Synth. Catal. 18/2016)

By  

ADVANCED SYNTHESIS & CATALYSIS, Vol. 358, Iss. 18, 2016-09 ,pp. : 2861-2861

John Wiley & Sons Inc

Access to resources Recommend Favorite

Catalytic Asymmetric Addition of Meldrum’s Acid, Malononitrile, and 1,3‐Dicarbonyls to ortho‐Quinone Methides Generated In Situ Under Basic Conditions

By  

CHEMISTRY - A EUROPEAN JOURNAL, Vol. 21, Iss. 16, 2015-04 ,pp. : 6037-6041

John Wiley & Sons Inc

Access to resources Recommend Favorite

N,N′‐Dioxide/Nickel(II)‐Catalyzed Asymmetric Inverse‐Electron‐Demand Hetero‐Diels–Alder Reaction of β,γ‐Unsaturated α‐Ketoesters with Enecarbamates

By  

CHEMISTRY - A EUROPEAN JOURNAL, Vol. 20, Iss. 50, 2014-12 ,pp. : 16753-16758

John Wiley & Sons Inc

Access to resources Recommend Favorite