Mercury(II) Chloride-Mediated Cyclization-Rearrangement of O-Propargylglycolaldehyde Dithioacetals to 3-Pyranone Dithioketals: An Expeditious Access to 3-Pyranones
EPrints@IICB
View Archive InfoField | Value | |
Title |
Mercury(II) Chloride-Mediated Cyclization-Rearrangement of O-Propargylglycolaldehyde Dithioacetals to 3-Pyranone Dithioketals: An Expeditious Access to 3-Pyranones |
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Creator |
Ghorai, Subir
Bhattacharjya, Anup |
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Subject |
Chemistry
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Description |
O-Propargyl glycolaldehyde dithioacetals undergo a unique cyclization-rearrangement in the presence of mercuric chloride and calcium carbonate to afford 3-pyranones exclusively or along with 2,5-dihydrofuran-3-carboxaldehydes via their dithioketals and dithioacetals |
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Publisher |
American Chemical Society
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Date |
2005
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Type |
Article
PeerReviewed |
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Format |
application/pdf
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Identifier |
http://www.eprints.iicb.res.in/582/1/ORGANIC_LETTERS__7(_2_)207%2D210;2005[102].pdf
Ghorai, Subir and Bhattacharjya, Anup (2005) Mercury(II) Chloride-Mediated Cyclization-Rearrangement of O-Propargylglycolaldehyde Dithioacetals to 3-Pyranone Dithioketals: An Expeditious Access to 3-Pyranones. Organic Letters, 7 (2). pp. 207-210. |
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Relation |
http://dx.doi.org/10.1021/ol047893a CCC: $30.25
http://www.eprints.iicb.res.in/582/ |
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