Synthesis of CBI-PDE-I-dimer, the benzannelated analog of CC-1065
PA Aristoff, PD Johnson
Index: Aristoff, Paul A.; Johnson, Paul D. Journal of Organic Chemistry, 1992 , vol. 57, # 23 p. 6234 - 6239
Full Text: HTML
Citation Number: 65
Abstract
A practical synthesis of CBI (2), utilizing inexpensive starting materials, waa developed and applied to the synthesis of benzannelated analogs of CC-1065, in particular CBI-PDE-I- dimer (13) and CBI-bis-indole (17). While a Sharplea asymmetric dihydroxylation reaction proved effective at providing optically active intermediates, a more classical resolution procedure waa used to prepare materials of higher optical purity. A novel cyclization ...
Related Articles:
[Parker, Kathlyn A.; Coburn, Craig A.; Johnson, Paul D.; Aristoff, Paul Journal of Organic Chemistry, 1992 , vol. 57, # 20 p. 5547 - 5550]
[Parker, Kathlyn A.; Coburn, Craig A.; Johnson, Paul D.; Aristoff, Paul Journal of Organic Chemistry, 1992 , vol. 57, # 20 p. 5547 - 5550]
[Parker, Kathlyn A.; Coburn, Craig A.; Johnson, Paul D.; Aristoff, Paul Journal of Organic Chemistry, 1992 , vol. 57, # 20 p. 5547 - 5550]