Mercury(II) Chloride-Mediated Cyclization-Rearrangement of O-Propargylglycolaldehyde Dithioacetals to 3-Pyranone Dithioketals: An Expeditious Access to 3-Pyranones
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | 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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