Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides

A. K. Prasad, Neerja Kalra, Y. Yadav, R. Kumar, S. K. Sharma, S Patkar, L. Lange, Jesper Wengel, Virinder S. Parmar

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Resumé

Lipozyme® TL IM immobilized on silica catalyses the deacylation of 4-C-acyloxymethyl-3,5-di-O-acyl-1,2-O-(1-methylethylidene)-β-L-threo-pentofuranose to form 3,5-di-O-acyl-4-C-hydroxymethyl-1,2-O-(1-methylethylidene)-α-D-xylo-pentofuranose in a highly selective and efficient manner.
OriginalsprogEngelsk
TidsskriftChemical Communications
Vol/bind2007
Udgave nummer25
Sider (fra-til)2616-2617
ISSN1359-7345
DOI
StatusUdgivet - 2007

Fingeraftryk

Lipases
Lipase
Silicon Dioxide
Silica
Lipozyme

Citer dette

Prasad, A. K., Kalra, N., Yadav, Y., Kumar, R., Sharma, S. K., Patkar, S., ... Parmar, V. S. (2007). Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides. Chemical Communications, 2007(25), 2616-2617. https://doi.org/10.1039/B618426J
Prasad, A. K. ; Kalra, Neerja ; Yadav, Y. ; Kumar, R. ; Sharma, S. K. ; Patkar, S ; Lange, L. ; Wengel, Jesper ; Parmar, Virinder S. / Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides. I: Chemical Communications. 2007 ; Bind 2007, Nr. 25. s. 2616-2617.
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title = "Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides",
abstract = "Lipozyme{\circledR} TL IM immobilized on silica catalyses the deacylation of 4-C-acyloxymethyl-3,5-di-O-acyl-1,2-O-(1-methylethylidene)-β-L-threo-pentofuranose to form 3,5-di-O-acyl-4-C-hydroxymethyl-1,2-O-(1-methylethylidene)-α-D-xylo-pentofuranose in a highly selective and efficient manner.",
author = "Prasad, {A. K.} and Neerja Kalra and Y. Yadav and R. Kumar and Sharma, {S. K.} and S Patkar and L. Lange and Jesper Wengel and Parmar, {Virinder S.}",
year = "2007",
doi = "10.1039/B618426J",
language = "English",
volume = "2007",
pages = "2616--2617",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
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Prasad, AK, Kalra, N, Yadav, Y, Kumar, R, Sharma, SK, Patkar, S, Lange, L, Wengel, J & Parmar, VS 2007, 'Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides', Chemical Communications, bind 2007, nr. 25, s. 2616-2617. https://doi.org/10.1039/B618426J

Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides. / Prasad, A. K.; Kalra, Neerja; Yadav, Y.; Kumar, R.; Sharma, S. K.; Patkar, S; Lange, L.; Wengel, Jesper; Parmar, Virinder S.

I: Chemical Communications, Bind 2007, Nr. 25, 2007, s. 2616-2617.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

TY - JOUR

T1 - Deacylation studies on furanose triesters using an immobilized lipase: synthesis of a key precursor for bicyclonucleosides

AU - Prasad, A. K.

AU - Kalra, Neerja

AU - Yadav, Y.

AU - Kumar, R.

AU - Sharma, S. K.

AU - Patkar, S

AU - Lange, L.

AU - Wengel, Jesper

AU - Parmar, Virinder S.

PY - 2007

Y1 - 2007

N2 - Lipozyme® TL IM immobilized on silica catalyses the deacylation of 4-C-acyloxymethyl-3,5-di-O-acyl-1,2-O-(1-methylethylidene)-β-L-threo-pentofuranose to form 3,5-di-O-acyl-4-C-hydroxymethyl-1,2-O-(1-methylethylidene)-α-D-xylo-pentofuranose in a highly selective and efficient manner.

AB - Lipozyme® TL IM immobilized on silica catalyses the deacylation of 4-C-acyloxymethyl-3,5-di-O-acyl-1,2-O-(1-methylethylidene)-β-L-threo-pentofuranose to form 3,5-di-O-acyl-4-C-hydroxymethyl-1,2-O-(1-methylethylidene)-α-D-xylo-pentofuranose in a highly selective and efficient manner.

U2 - 10.1039/B618426J

DO - 10.1039/B618426J

M3 - Journal article

VL - 2007

SP - 2616

EP - 2617

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 25

ER -