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PHOTOREARRANGEMENT OF 2,3-DIMETHYL-4,5-DIHYDROFURAN AND 2-METHYL-4,5-DIHYDROFURAN
Irradiation of an ether solution of the title compounds with a medium-pressure mercury are gave in each case a rearrangement reaction, with formation of an acetyl cyclopropane isomer as the major product. This reaction is similar to that induced thermally at 450°.
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Published in: | Canadian journal of chemistry 1965-05, Vol.43 (5), p.1417-1418 |
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Format: | Article |
Language: | English |
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cites | cdi_FETCH-LOGICAL-c221t-a5594f503dfe9cb034d212a7dc7c4e04738f6a6c310457fe70f3f7623213e8b03 |
container_end_page | 1418 |
container_issue | 5 |
container_start_page | 1417 |
container_title | Canadian journal of chemistry |
container_volume | 43 |
creator | McGreer, Donald E Vinje, Magnus G McDaniel, Robert S |
description | Irradiation of an ether solution of the title compounds with a medium-pressure mercury are gave in each case a rearrangement reaction, with formation of an acetyl cyclopropane isomer as the major product. This reaction is similar to that induced thermally at 450°. |
doi_str_mv | 10.1139/v65-191 |
format | article |
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ispartof | Canadian journal of chemistry, 1965-05, Vol.43 (5), p.1417-1418 |
issn | 0008-4042 1480-3291 |
language | eng |
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source | EZB-FREE-00999 freely available EZB journals |
title | PHOTOREARRANGEMENT OF 2,3-DIMETHYL-4,5-DIHYDROFURAN AND 2-METHYL-4,5-DIHYDROFURAN |
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