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Chemo-enzymatic syntheses of natural and unnatural 2'-deoxynucleosides
Author(s) -
H. Komatsu,
Hirokazu Awano,
Hiroki Ishibashi,
T Oikawa,
Ichiro Ikeda,
Tadashi Araki
Publication year - 2003
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/3.1.101
Subject(s) - chemistry , enzyme , biochemistry
A chemo-enzymatic method for preparations of natural and unnatural deoxynucleosides was developed. The method consists of chemical synthesis of natural and unnatural deoxyribose 1-phosphates and their enzymatic conversion to deoxynucleosides. A highly stereoselective synthesis of 2-deoxyribose 1-phosphate was first achieved by an unprecedented application of crystallization-induced asymmetric transformation. Additionally, we first discovered a 2'-deoxycytidine producing enzyme. The discovery and the development of a scalable synthetic process of 2-deoxyribose 1-phosphate enabled us to manufacture all four natural 2'-deoxynucleosides practically. The methodology was applied to the synthesis of 2',3'-dideoxy-3'-fluoroguanosine via synthetic 2,3-dideoxy-3-fluororibose 1-phosphate.

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