Allylation and propargylation of aldehydes mediated by in situ generated zinc from the redox couple of Al and ZnCl2 in 2N HCl
A simple one pot allylation and propargylation of aldehydes mediated by zinc(0), which is in situ generated from the redox couple of Al and ZnCl2 in 2N HCl, is demonstrated to afford the corresponding homoallyl and homopropargyl alcohols with excellent yields.
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Published in | New journal of chemistry Vol. 45; no. 16; pp. 7163 - 7173 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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28.04.2021
Royal Society of Chemistry |
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Abstract | A simple one pot allylation and propargylation of aldehydes mediated by zinc(0), which is in situ generated from the redox couple of Al and ZnCl2 in 2N HCl, is demonstrated to afford the corresponding homoallyl and homopropargyl alcohols with excellent yields. |
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AbstractList | A simple one pot allylation and propargylation of aldehydes mediated by zinc(0), which is in situ generated from the redox couple of Al and ZnCl2 in 2N HCl, is demonstrated to afford the corresponding homoallyl and homopropargyl alcohols with excellent yields. |
Author | Roy, Ujjal Kanti Hajra, Partha Pratim Mondal, Bibhas Adhikari, Utpal |
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Keywords | HALIDES KETONES TETRAPROPARGYLIC STANNANES TRANSMETALATION AQUEOUS-MEDIA HOMOALLYLIC ALCOHOLS CARBONYL ALLYLATION REACTIVITY EFFICIENT SOLVENT |
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Snippet | A simple one pot allylation and propargylation of aldehydes mediated by zinc(0), which is in situ generated from the redox couple of Al and ZnCl2 in 2N HCl, is... |
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SubjectTerms | Alcohols Aldehydes Allyl compounds Chemical reactions Chemistry Chemistry, Multidisciplinary Physical Sciences Science & Technology Zinc chloride |
Title | Allylation and propargylation of aldehydes mediated by in situ generated zinc from the redox couple of Al and ZnCl2 in 2N HCl |
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