Mehta, Goverdhan and Shinde, Harish M (2005) Enantioselective total synthesis of bioactive natural product (+)-Sch642305: a structurally novel inhibitor of bacterial DNA primase and HIV-1 Tat transactivation. In: Chemical Communications (29). pp. 3703-3705.
The total synthesis of the bioactive natural product (+)-Sch 642305 has been achieved from a readily available chiral building block using an RCM protocol to construct the key decalactone moiety; our approach is notable for its built-in flexibility and is diversity oriented.
|Item Type:||Journal Article|
|Additional Information:||Copyright for this article belongs to Royal Society of Chemistry.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||24 Aug 2005|
|Last Modified:||19 Sep 2010 04:19|
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