(E)-(4R)-Dibenzyloxy HEX-2-ENAL 1-(ethylene acetal): A new chiral compound useful for eicosanoid synthesis

Jean Paul Lellouche; Patrick Quinton

doi:10.1080/00397919408010205

(E)-(4R)-Dibenzyloxy HEX-2-ENAL 1-(ethylene acetal): A new chiral compound useful for eicosanoid synthesis

Jean Paul Lellouche
, Patrick Quinton

Serv. des Molecules Marquees

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

The preparation of the new six carbon multifunctionalized chiral synthon 4, useful for eicosanoid synthesis, was achieved employing the Perlin hydrolysis reaction of 3,4,6-tri-O-benzyl-D-Glucal 6 in the key step.

Original language	English
Pages (from-to)	1979-1988
Number of pages	10
Journal	Synthetic Communications
Volume	24
Issue number	14
DOIs	https://doi.org/10.1080/00397919408010205
State	Published - 1 Jul 1994
Externally published	Yes

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10.1080/00397919408010205

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@article{6d5e43c15d25476ea9e650213c83169b,

title = "(E)-(4R)-Dibenzyloxy HEX-2-ENAL 1-(ethylene acetal): A new chiral compound useful for eicosanoid synthesis",

abstract = "The preparation of the new six carbon multifunctionalized chiral synthon 4, useful for eicosanoid synthesis, was achieved employing the Perlin hydrolysis reaction of 3,4,6-tri-O-benzyl-D-Glucal 6 in the key step.",

author = "Lellouche, \{Jean Paul\} and Patrick Quinton",

year = "1994",

month = jul,

day = "1",

doi = "10.1080/00397919408010205",

language = "אנגלית",

volume = "24",

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publisher = "Taylor and Francis Ltd.",

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T1 - (E)-(4R)-Dibenzyloxy HEX-2-ENAL 1-(ethylene acetal)

T2 - A new chiral compound useful for eicosanoid synthesis

AU - Lellouche, Jean Paul

AU - Quinton, Patrick

PY - 1994/7/1

Y1 - 1994/7/1

N2 - The preparation of the new six carbon multifunctionalized chiral synthon 4, useful for eicosanoid synthesis, was achieved employing the Perlin hydrolysis reaction of 3,4,6-tri-O-benzyl-D-Glucal 6 in the key step.

AB - The preparation of the new six carbon multifunctionalized chiral synthon 4, useful for eicosanoid synthesis, was achieved employing the Perlin hydrolysis reaction of 3,4,6-tri-O-benzyl-D-Glucal 6 in the key step.

UR - https://www.scopus.com/pages/publications/0028301359

U2 - 10.1080/00397919408010205

DO - 10.1080/00397919408010205

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SN - 0039-7911

VL - 24

SP - 1979

EP - 1988

JO - Synthetic Communications

JF - Synthetic Communications

IS - 14

ER -

(E)-(4R)-Dibenzyloxy HEX-2-ENAL 1-(ethylene acetal): A new chiral compound useful for eicosanoid synthesis

Abstract

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