Please use this identifier to cite or link to this item: http://dri.iictindia.org/jspui/handle/123456789/2180
Title: Efficient regioselective ring opening of oxiranes with thioacids in the presence of β-cyclodextrin in water
Authors: Srinivas, B
Sridhar, R
Surendra, K
Krishnaveni, N.S
PavanKumar, V
Nageswar, Y.V.D
RamaRao, K
Keywords: β-Cyclodextrin
Oxiranes
Thio acids
Water
Issue Date: 2006
Publisher: Taylor & Francis
Citation: Synthetic communications, Vol. 36(22-24), 3455-3459p
Abstract: A mild and convenient synthesis of /3-hydroxy thioesters has been achieved by the regioselective ring opening of oxiranes using thioacetic acid and thiobenzoic acid in the presence of β-cyclodextrin in water at room temperature. β-Hydroxy thioesters are realized in high yields, and /3-cyclodextrin can also be recovered and reused.
URI: http://hdl.handle.net/123456789/2180
ISSN: 0039-7911
Appears in Collections:Natural Product Chemistry(Org-I)

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