Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors

Eugene A. Mash; Jeffrey B. Arterburn; James A. Fryling

doi:10.1016/S0040-4039(01)93919-X

Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors

Eugene A. Mash
, Jeffrey B. Arterburn
, James A. Fryling

Chemistry and Biochemistry

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

8 Scopus citations

Abstract

A general chromatographic separation of furanosides and pyranosides derived from esters of lactic acid is disclosed. Application of this separation methodology to rapid syntheses of the diastereomers of (S)-methyl lactyl 4-deoxyribopyranose is described.

Original language	English (US)
Pages (from-to)	7145-7148
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	51
DOIs	https://doi.org/10.1016/S0040-4039(01)93919-X
State	Published - 1989

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)93919-X

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title = "Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors",

abstract = "A general chromatographic separation of furanosides and pyranosides derived from esters of lactic acid is disclosed. Application of this separation methodology to rapid syntheses of the diastereomers of (S)-methyl lactyl 4-deoxyribopyranose is described.",

author = "Mash, \{Eugene A.\} and Arterburn, \{Jeffrey B.\} and Fryling, \{James A.\}",

year = "1989",

doi = "10.1016/S0040-4039(01)93919-X",

language = "English (US)",

volume = "30",

pages = "7145--7148",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "51",

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T1 - Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors

AU - Mash, Eugene A.

AU - Arterburn, Jeffrey B.

AU - Fryling, James A.

PY - 1989

Y1 - 1989

N2 - A general chromatographic separation of furanosides and pyranosides derived from esters of lactic acid is disclosed. Application of this separation methodology to rapid syntheses of the diastereomers of (S)-methyl lactyl 4-deoxyribopyranose is described.

AB - A general chromatographic separation of furanosides and pyranosides derived from esters of lactic acid is disclosed. Application of this separation methodology to rapid syntheses of the diastereomers of (S)-methyl lactyl 4-deoxyribopyranose is described.

UR - https://www.scopus.com/pages/publications/0024806961

UR - https://www.scopus.com/pages/publications/0024806961#tab=citedBy

U2 - 10.1016/S0040-4039(01)93919-X

DO - 10.1016/S0040-4039(01)93919-X

M3 - Article

AN - SCOPUS:0024806961

SN - 0040-4039

VL - 30

SP - 7145

EP - 7148

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 51

ER -

Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors

Abstract

ASJC Scopus subject areas

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