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Rao et al., 1990 - Google Patents

Regio-and chemoselective conjugate 1, 4-reduction of α-oxoketene dithioacetals with sodium borohydride and sodium cyanoborohydride

Rao et al., 1990

Document ID
5961831222874476501
Author
Rao C
Chakrasali R
Ila H
Junjappa H
Publication year
Publication venue
Tetrahedron

External Links

Snippet

Theα-oxoketene dithioacetals 1 are shown to undergo conjugate 1, 4-reduction in highly regio-and chemoselective manner with sodium borohydride in acetic acid to afford the corresponding β-oxodithioacetals 5 in good yields. These results have been rationalized …
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    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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