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Novel Iodine Reagent System for Regioselective Cleavage of Epoxides to Alcohols
Epoxides are converted regioselectively to corresponding higher substituted alcohols with greater yields using diphosphorus tetraiodide (P 2 I 4 ) as a reducing agent and a catalytic amount of tetraethylammonium bromide at room temperature.
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Published in: | Synthetic communications 2010-06, Vol.40 (14), p.2108-2112 |
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Language: | English |
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cited_by | cdi_FETCH-LOGICAL-c373t-2b866dafc2f0162a231651f183518cf3b440a285c43f0dc61db0d6a87d101aa3 |
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cites | cdi_FETCH-LOGICAL-c373t-2b866dafc2f0162a231651f183518cf3b440a285c43f0dc61db0d6a87d101aa3 |
container_end_page | 2112 |
container_issue | 14 |
container_start_page | 2108 |
container_title | Synthetic communications |
container_volume | 40 |
creator | Telvekar, Vikas N. Rane, Rajesh A. |
description | Epoxides are converted regioselectively to corresponding higher substituted alcohols with greater yields using diphosphorus tetraiodide (P
2
I
4
) as a reducing agent and a catalytic amount of tetraethylammonium bromide at room temperature. |
doi_str_mv | 10.1080/00397910903219492 |
format | article |
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ispartof | Synthetic communications, 2010-06, Vol.40 (14), p.2108-2112 |
issn | 0039-7911 1532-2432 |
language | eng |
recordid | cdi_proquest_journals_856344736 |
source | Taylor and Francis Science and Technology Collection |
subjects | Alcohols diphosphorus tetraiodide epoxides reduction tetraethylammonium bromide |
title | Novel Iodine Reagent System for Regioselective Cleavage of Epoxides to Alcohols |
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