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Charette Asymmetric Cyclopropanation

Charette Asymmetric Cyclopropanation

Mechanism of the Charette Asymmetric Cyclopropanation

Reference



Sample reactions

This reaction is from the synthesis of U-106305 by André B. Charette. Show me the full synthesis.

Reactant structure
Reagent structureEt2Zn, CH2I2
Reaction arrow head
DME, CH2Cl2
-20 °C to RT, 8.5 h
90%
Product structure

This reaction is from the synthesis of U-106305 by André B. Charette. Show me the full synthesis.

Reactant structure
Reagent structureEt2Zn, CH2I2
Reaction arrow head
DME, CH2Cl2
-20 °C to RT, 8.5 h
90%
Product structure

This reaction is from the synthesis of Pseudolaric Acid B by Barry M. Trost. Show me the full synthesis.

Reactant structure
Reagent structureEt2Zn, CH2I2
Reaction arrow head
CH2Cl2, DME
-10 °C to RT, 14.5 h
91%
Product structure

This reaction is from the synthesis of Doliculide by Arun K. Ghosh. Show me the full synthesis.

Reactant structure
Reagent structureEt2Zn, CH2I2
Reaction arrow head
CH2Cl2, DME
-15 °C, 8 h
99%
Product structure

This reaction is from the synthesis of Doliculide by Arun K. Ghosh. Show me the full synthesis.

Reactant structure
Reagent structureEt2Zn, CH2I2
Reaction arrow head
CH2Cl2, DME
-15 °C, 8 h
96%
Product structure

This reaction is from the synthesis of U-106305 by André B. Charette. Show me the full synthesis.

Reactant structure
Reagent structureEt2Zn, CH2I2
Reaction arrow head
DME, CH2Cl2
-20 °C to RT, 8.5 h
Product structure
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