Mercury(II) chloride-mediated cyclization - Rearrangement of O-propargylglycolaldehyde dithioacetals to 3-pyranone dithioketals: An expeditious access to 3-pyranones
Metadata of CSIR Papers
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, S
Bhattacharjya, A |
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| Subject |
Chemistry, Organic
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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 |
AMER CHEMICAL SOCWASHINGTON1155 16TH ST, NW, WASHINGTON, DC 20036 USA
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| Date |
2011-09-20T12:12:00Z
2011-09-20T12:12:00Z 2005 |
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| Type |
Article
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| Identifier |
ORGANIC LETTERS
1523-7060 http://hdl.handle.net/123456789/14080 |
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| Language |
English
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