Charette Asymmetric Cyclopropanation
Mechanism of the Charette Asymmetric Cyclopropanation
Reference
| Original reference | J. Am. Chem. Soc. 1994, 116, 2651. |
|---|
Sample reactions
This step is from the synthesis of U-106305 by André B. Charette. Show me the full synthesis.

Et2Zn, CH2I2
-20 °C to RT, 8.5 h
90 %

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

Et2Zn, CH2I2
-20 °C to RT, 8.5 h
90 %

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

Et2Zn, CH2I2
-10 °C to RT, 14.5 h
91 %

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

Et2Zn, CH2I2
-15 °C, 8 h
99 %

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

Et2Zn, CH2I2
-15 °C, 8 h
96 %
