A mild and convenient deprotection of 4-phenyl 1,3-dioxolane derivatives under catalytic hydrogenation

Synthetic Communications

Volumn 27, Issue 15, 1997, Pages 2691-2694

  Chandrasekhar, S ^a   Muralidhar, B ^a   Sarkar, Sanjita ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; CARBONYL DERIVATIVE;

ARTICLE; CATALYSIS; CHROMATOGRAPHY; DRUG SYNTHESIS; HYDROGENATION; PH;

EID: 1842288567     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919708004137     Document Type: Article

References (9)

1. Greene, T.W. Protective groups in organic synthesis; John Wiley & Sons, Inc.; 1980.
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3. Katritzky, A.R.; Fan, W.Q; Li, Q.L. Tetrahedron Lett., 1987, 28, 1195.
4. Zufan Wu.; Mootoo, D.R.; Fraser Reid, B. Tetrahedron Lett., 1988, 29, 6549.
5. Lillie, B.M.; Avery, M.A. Tetrahedron Lett., 1994, 35, 969.
6. Masui, M.; Kawaguchi, T.; Ozaki, S. JCS Chem. Comm., 1985, 1484.
7. 2,4-benzodioxepines are known to be cleaved under catalytic hydrogenation, however, the present methodology offers advantages in preparation of chiral diols from styrene by asymetric dihydroxylation for a possible kinetic resolution of prochiral aldehydes.
8. Machinaga, N.; Kibayashi, C. Tetrahedron Lett., 1989, 30, 4165.
9. All products were characterised by comparing with standard sample.