134931-85-4Relevant academic research and scientific papers
ASYMMETRIC ALDOL REACTIONS USING CHIRAL BORON REAGENTS: APPLICATION TO THE SYNTHESIS OF TIRANDAMYCIN A
Paterson, Ian,Lister, M. Anne,Ryan, Glen R.
, p. 1749 - 1752 (2007/10/02)
The bicyclic acetal 1, a key intermediate in previous synthetic studies on tirandamycin A, has been prepared in enantiomerically pure form starting from the (R)-ethylketone 2 and the aldehyde 3.A reagent controlled aldol reaction using (-)-(Ipc)2BOTf sele
Synthesis of the dioxabicyclononane unit of tirandamycin
Kelly,Chandrakumar,Cutting,et al.
, p. 2173 - 2176 (2007/10/02)
A seven-step synthesis of (±)-3b, an advanced, common intermediated for construction of the dioxabicyclononane units of both tirandamycin and streptolydigin is described. Conversion of 3b to the fully developed fragment of tirandamycin is also reported.
