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Rearrangement of p-methoxybenzyl-protected allylic alcohols to aldehydes
Home
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Rearrangement of p-methoxybenzyl-protected allylic alcohols to aldehydes
Rearrangement of p-methoxybenzyl-protected allylic alcohols to aldehydes
JW
Johan Wennerberg
Johan Wennerberg
LE
Lars Eklund
Lars Eklund
MP
Magnus Polla
Magnus Polla
TF
Torbjörn Frejd
Torbjörn Frejd
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1 January 1997
journal article
research article
Published by
Royal Society of Chemistry (RSC)
in
Chemical Communications
No. 5
,
p.
445-446
https://doi.org/10.1039/a608020k
Abstract
Allyl p-methoxybenzyl ethers undergo an acid-catalysed 1,4-rearrangement to give p-methoxyphenylbutyraldehyde derivatives, which can be ring-closed to give substituted naphthalene derivatives.
Keywords
METHOXYBENZYL
METHOXYPHENYLBUTYRALDEHYDE
ALCOHOLS
SUBSTITUTED
ALLYLIC
ALDEHYDES
ETHERS
CATALYSED
NAPHTHALENE
UNDERGO
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Cited by 6 articles