An expeditious approach to trisubstituted chiral tetrahydrofurans

Fazila Iqbal; Mohammed Saleh Shekhani; Abdul Malik; Masood Parvez; Uzma Riaz; Zulfiqar Ali; Khalid Mohammed Khan

doi:10.1515/znb-2000-3-413

An expeditious approach to trisubstituted chiral tetrahydrofurans

Fazila Iqbal
, Mohammed Saleh Shekhani
, Abdul Malik
, Masood Parvez
, Uzma Riaz
, Zulfiqar Ali
, Khalid Mohammed Khan

Chemistry

University of Karachi
University of Calgary

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

1 Scopus citations

Abstract

Ozonolysis of 3,6-anhydro-4-O-(p-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the corresponding derivatives 10 and 12, respectively.

Original language	English
Pages (from-to)	317-320
Number of pages	4
Journal	Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences
Volume	55
Issue number	3-4
DOIs	https://doi.org/10.1515/znb-2000-3-413
State	Published - 2000

Keywords

Asymmetric Synthesis
Chiral Tetrahydrofurans
D-Galactose
D-Glucose

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title = "An expeditious approach to trisubstituted chiral tetrahydrofurans",

abstract = "Ozonolysis of 3,6-anhydro-4-O-(p-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the corresponding derivatives 10 and 12, respectively.",

keywords = "Asymmetric Synthesis, Chiral Tetrahydrofurans, D-Galactose, D-Glucose",

author = "Fazila Iqbal and Shekhani, \{Mohammed Saleh\} and Abdul Malik and Masood Parvez and Uzma Riaz and Zulfiqar Ali and Khan, \{Khalid Mohammed\}",

year = "2000",

doi = "10.1515/znb-2000-3-413",

language = "English",

volume = "55",

pages = "317--320",

journal = "Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences",

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T1 - An expeditious approach to trisubstituted chiral tetrahydrofurans

AU - Iqbal, Fazila

AU - Shekhani, Mohammed Saleh

AU - Malik, Abdul

AU - Parvez, Masood

AU - Riaz, Uzma

AU - Ali, Zulfiqar

AU - Khan, Khalid Mohammed

PY - 2000

Y1 - 2000

N2 - Ozonolysis of 3,6-anhydro-4-O-(p-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the corresponding derivatives 10 and 12, respectively.

AB - Ozonolysis of 3,6-anhydro-4-O-(p-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the corresponding derivatives 10 and 12, respectively.

KW - Asymmetric Synthesis

KW - Chiral Tetrahydrofurans

KW - D-Galactose

KW - D-Glucose

UR - https://www.scopus.com/pages/publications/0040199934

U2 - 10.1515/znb-2000-3-413

DO - 10.1515/znb-2000-3-413

M3 - Article

AN - SCOPUS:0040199934

SN - 0932-0776

VL - 55

SP - 317

EP - 320

JO - Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences

JF - Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences

IS - 3-4

ER -

An expeditious approach to trisubstituted chiral tetrahydrofurans

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Keywords

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