Stereospecific solid-state NaBH4-promoted reduction of 1-methylpentacyclo[5.4.0.0(2,6).0(3,10).0(5,9)]undecane-8,11-dione
| Data(s) |
01/11/1997
|
|---|---|
| Resumo |
NaBH4 reduction of a cage dione proceeds in a stereospecific fashion to give the endo,endo-diol. This reactivity is related to the crystal structure. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/38483/1/Stereospecific_solid-state.pdf Bott, SG and Marchand, AP and Xing, DX and Shukla, R and Obrey, SJ and Venkatesan, K and Moorthy, JN (1997) Stereospecific solid-state NaBH4-promoted reduction of 1-methylpentacyclo[5.4.0.0(2,6).0(3,10).0(5,9)]undecane-8,11-dione. In: Journal of Chemical Crystallography, 27 (11). pp. 661-665. |
| Publicador |
Springer |
| Relação |
http://www.springerlink.com/content/w31q4u083t15273j/ http://eprints.iisc.ernet.in/38483/ |
| Palavras-Chave | #Others |
| Tipo |
Journal Article PeerReviewed |
