Lewis Acid Catalyzed Tandem Diels—Alder Reaction/Retro-Claisen Rearrangement as an Equivalent of the Inverse Electron Demand Hetero Diels—Alder Reaction.

ChemInform Abstract: Lewis Acid Catalyze

ChemInform Abstract: Lewis Acid Catalyzed Inverse-Electron-Demand Diels—Alder Reaction of Tropones.

✍ Pingfan Li; Hisashi Yamamoto 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 56 KB 👁 1 views

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ChemInform Abstract: Lewis Acid Catalyze

ChemInform Abstract: Lewis Acid Catalyzed Inverse Electron-Demand Diels—Alder Reaction of 1,2-Diazines.

✍ Simon N. Kessler; Hermann A. Wegner 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Asymmetric Inverse-Electron-Demand Heter

Asymmetric Inverse-Electron-Demand Hetero-Diels–Alder Reaction of Six-membered Cyclic Ketones: An Enamine/Metal Lewis Acid Bifunctional Approach

✍ Dr. Zhenghu Xu; Dr. Lu Liu; Prof. Dr. Kraig Wheeler; Prof. Dr. Hong Wang 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 372 KB 👁 1 views

The combination of organocatalysis with metal catalysis has emerged as a potentially powerful tool in organic synthesis. [1] This new concept aims to achieve organic transformations that cannot be accessed by organocatalysis or metal catalysis alone. In our effort to combine organo-enamine catalysis

Asymmetric Inverse-Electron-Demand Heter

Asymmetric Inverse-Electron-Demand Hetero-Diels–Alder Reaction of Six-membered Cyclic Ketones: An Enamine/Metal Lewis Acid Bifunctional Approach

✍ Dr. Zhenghu Xu; Dr. Lu Liu; Prof. Dr. Kraig Wheeler; Prof. Dr. Hong Wang 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 382 KB 👁 1 views

The combination of organocatalysis with metal catalysis has emerged as a potentially powerful tool in organic synthesis. [1] This new concept aims to achieve organic transformations that cannot be accessed by organocatalysis or metal catalysis alone. In our effort to combine organo-enamine catalysis

The First Catalytic Inverse-Electron Dem

The First Catalytic Inverse-Electron Demand hetero-Diels—Alder Reaction of Nitroso Alkenes Using Pyrrolidine as an Organocatalyst.

✍ Tobias C. Wabnitz; Steen Saaby; Karl Anker Joergensen 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 186 KB 👁 1 views

Lewis Acid Induced Tandem Diels—Alder Re

Lewis Acid Induced Tandem Diels—Alder Reaction/Ring Expansion as an Equivalent of a [4 + 3] Cycloaddition.

✍ Huw M. L. Davies; Xing Dai 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 167 KB 👁 1 views

Lewis Acid Catalyzed Tandem Diels—Alder Reaction/Retro-Claisen Rearrangement as an Equivalent of the Inverse Electron Demand Hetero Diels—Alder Reaction.

✦ Synopsis

Abstract