Stereoselective hydrogenation of R -q-pulegone and 2S,5R -y-menthone in presence of b-cyclodextrin and its derivatives
IR@CSIR-CFTRI
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Relation |
http://ir.cftri.com/1220/
JMC_03_99 |
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Title |
Stereoselective hydrogenation of R -q-pulegone and 2S,5R -y-menthone in presence of b-cyclodextrin and its derivatives |
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Creator |
Palaniswami, Ravi
Ramaswamy, Ravichandran Soundar, Divakar |
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Subject |
12 Aromatic Chemistry
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Description |
Stereoselective hydrogenation of R - q -pulegone and 2S,5R - y -menthone over Raney nickel at room temperature with dilute and concentrated alkali in presence of b-cyclodextrin and its derivatives was studied. The effect of alkali and b-cyclodextrin and its derivatives on the modification of the yield and the proportion of epimeric alcohols formed were found to be the salient features of this reaction Scheme 1 .
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Date |
1999
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Type |
Article
PeerReviewed |
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Format |
application/pdf
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Language |
en
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Rights |
—
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Identifier |
http://ir.cftri.com/1220/1/Journal_of_Molecular_Catalysis_A_Chemical_148_1999_145-155.pdf
Palaniswami, Ravi and Ramaswamy, Ravichandran and Soundar, Divakar (1999) Stereoselective hydrogenation of R -q-pulegone and 2S,5R -y-menthone in presence of b-cyclodextrin and its derivatives. Journal of Molecular Catalysis A: Chemical, 148. pp. 145-155. |
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