Synthesis of optically active O-protected (S)- and (R)-3-hydroxyaldehydes

Suk Ku Kang; Hyun Sung Cho

doi:10.1016/S0040-4039(00)92630-3

Synthesis of optically active O-protected (S)- and (R)-3-hydroxyaldehydes

Suk Ku Kang
, Hyun Sung Cho

Department of Anesthesiology and Pain Medicine

Sungkyunkwan University

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

6 Scopus citations

Abstract

(S)-3-Formyloxyaldehydes, chiral synthons for natural product synthesis were synthesized via highly stereoselective hydrogenation of the unsaturated furanose ring system derived from D-glucose or D-xylose. Alternatively, (R)-3-formyloxyaldehydes were prepared via deoxygenation of 3-hydroxyfuranoses derived from D-glucose or D-xylose.

Original language	English
Pages (from-to)	367-370
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	3
DOIs	https://doi.org/10.1016/S0040-4039(00)92630-3
State	Published - 14 Jan 1991

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title = "Synthesis of optically active O-protected (S)- and (R)-3-hydroxyaldehydes",

abstract = "(S)-3-Formyloxyaldehydes, chiral synthons for natural product synthesis were synthesized via highly stereoselective hydrogenation of the unsaturated furanose ring system derived from D-glucose or D-xylose. Alternatively, (R)-3-formyloxyaldehydes were prepared via deoxygenation of 3-hydroxyfuranoses derived from D-glucose or D-xylose.",

author = "Kang, \{Suk Ku\} and Cho, \{Hyun Sung\}",

year = "1991",

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doi = "10.1016/S0040-4039(00)92630-3",

language = "English",

volume = "32",

pages = "367--370",

journal = "Tetrahedron Letters",

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T1 - Synthesis of optically active O-protected (S)- and (R)-3-hydroxyaldehydes

AU - Kang, Suk Ku

AU - Cho, Hyun Sung

PY - 1991/1/14

Y1 - 1991/1/14

N2 - (S)-3-Formyloxyaldehydes, chiral synthons for natural product synthesis were synthesized via highly stereoselective hydrogenation of the unsaturated furanose ring system derived from D-glucose or D-xylose. Alternatively, (R)-3-formyloxyaldehydes were prepared via deoxygenation of 3-hydroxyfuranoses derived from D-glucose or D-xylose.

AB - (S)-3-Formyloxyaldehydes, chiral synthons for natural product synthesis were synthesized via highly stereoselective hydrogenation of the unsaturated furanose ring system derived from D-glucose or D-xylose. Alternatively, (R)-3-formyloxyaldehydes were prepared via deoxygenation of 3-hydroxyfuranoses derived from D-glucose or D-xylose.

UR - https://www.scopus.com/pages/publications/0026069387

U2 - 10.1016/S0040-4039(00)92630-3

DO - 10.1016/S0040-4039(00)92630-3

M3 - Article

AN - SCOPUS:0026069387

SN - 0040-4039

VL - 32

SP - 367

EP - 370

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 3

ER -

Synthesis of optically active O-protected (S)- and (R)-3-hydroxyaldehydes

Abstract

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