Syntheses of trans-SCH-A and cis-SCH-A via a stereodivergent cyclopropanation protocol.
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SCH-A and cis-SCH-A. This strategy encompasses a stereodivergent procedure for the preparation of syn- and anti-cyclopropane diastereoisomers in high dr from a common allylic carbamate precursor.
Bibliographic Details
Main Authors: |
Csatayová, K,
Davies, S,
Lee, J,
Ling, K,
Roberts, P,
Russell, A,
Thomson, J |
Format: | Journal article
|
Language: | English |
Published: |
2010
|