An efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O- isopropylidene-D-mannono-1,4-lactone

Tzenge Lien Shih; Jui Huang Tseng

doi:10.1016/j.tetlet.2003.12.113

An efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O- isopropylidene-D-mannono-1,4-lactone

Tzenge Lien Shih^*, Jui Huang Tseng

^*Corresponding author for this work

Tamkang University

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

1 Scopus citations

Abstract

We reported herein an efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone in five steps. The key feature of this method involved a one-pot, 'double inversion' procedure at the stereocenters of C-4 and C-5 of D-mannono-1,4-lactone to afford the target molecule.

Original language	English
Pages (from-to)	1789-1791
Number of pages	3
Journal	Tetrahedron Letters
Volume	45
Issue number	8
DOIs	https://doi.org/10.1016/j.tetlet.2003.12.113
State	Published - 16 02 2004
Externally published	Yes

Keywords

L-Allono-1,4-lactone

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10.1016/j.tetlet.2003.12.113

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abstract = "We reported herein an efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone in five steps. The key feature of this method involved a one-pot, 'double inversion' procedure at the stereocenters of C-4 and C-5 of D-mannono-1,4-lactone to afford the target molecule.",

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AU - Shih, Tzenge Lien

AU - Tseng, Jui Huang

PY - 2004/2/16

Y1 - 2004/2/16

N2 - We reported herein an efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone in five steps. The key feature of this method involved a one-pot, 'double inversion' procedure at the stereocenters of C-4 and C-5 of D-mannono-1,4-lactone to afford the target molecule.

AB - We reported herein an efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone in five steps. The key feature of this method involved a one-pot, 'double inversion' procedure at the stereocenters of C-4 and C-5 of D-mannono-1,4-lactone to afford the target molecule.

KW - L-Allono-1,4-lactone

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DO - 10.1016/j.tetlet.2003.12.113

M3 - 文章

AN - SCOPUS:0842326653

SN - 0040-4039

VL - 45

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 8

ER -

An efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O- isopropylidene-D-mannono-1,4-lactone

Abstract

Keywords

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