Stereoselective synthesis of the C1–C10 fragment of rhizoxin D
摘要:
A novel approach towards the synthesis of the C1-C10 fragment of the biologically active antimitotic agent rhizoxin D is described. The synthesis involves a stereoselective Michael addition reaction of lithium diallyl cuprate with an alpha,beta-unsaturated six membered lactone. (c) 2006 Elsevier Ltd. All rights reserved.
Stereoselective synthesis of the C1–C10 fragment of rhizoxin D
摘要:
A novel approach towards the synthesis of the C1-C10 fragment of the biologically active antimitotic agent rhizoxin D is described. The synthesis involves a stereoselective Michael addition reaction of lithium diallyl cuprate with an alpha,beta-unsaturated six membered lactone. (c) 2006 Elsevier Ltd. All rights reserved.
A novel approach towards the synthesis of the C1-C10 fragment of the biologically active antimitotic agent rhizoxin D is described. The synthesis involves a stereoselective Michael addition reaction of lithium diallyl cuprate with an alpha,beta-unsaturated six membered lactone. (c) 2006 Elsevier Ltd. All rights reserved.