Synthesis of both enantiomers of 1-phenylethane-1,2-diol via chirality transfer from bile acid derivatives
| Data(s) |
08/09/2000
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| Resumo |
Both enantiomers of 1-phenylethane-1,2-diol were synthesized with good to excellent enantioselectivities via selective reduction of the phenylglyoxalates derived from bile acids, followed by reductive cleavage. (C) 2000 Elsevier Science Ltd. All rights reserved. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/32109/1/both.pdf Bandyopadhyaya, AK and Sangeetha, NM and Radha, A and Maitra, Uday (2000) Synthesis of both enantiomers of 1-phenylethane-1,2-diol via chirality transfer from bile acid derivatives. In: Tetrahedron: Asymmetry, 11 (17). pp. 3463-3466. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/S0957-4166(00)00338-4 http://eprints.iisc.ernet.in/32109/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
