225108-20-3Relevant articles and documents
Silylation-mediated transesterification of O-phenyl H-phosphonothioates - A new entry to nucleoside H-phosphonothioate monoesters
Laven, Gaston,Nilsson, Johan,Stawinski, Jacek
, p. 5111 - 5114 (2007/10/03)
O-Phenyl H-phosphonothioate undergoes a facile transesterification with suitably protected nucleosides upon in situ silylation with tert- butyldiphenylsilyl chloride in pyridine/toluene to produce the corresponding 3′-H-phosphonothioates in good yields. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
Aryl H-Phosphonates. 12. Synthetic and 31P NMR Studies on the Preparation of Nucleoside H-Phosphonothioate and Nucleoside H-Phosphonodithioate Monoesters
Cieslak, Jacek,Jankowska, Jadwiga,Stawinski, Jacek,Kraszewski, Adam
, p. 7049 - 7054 (2007/10/03)
Transformation of nucleoside H-phosphonate monoesters into the corresponding H-phosphonothioate and H-phosphonodithioate derivatives and possible side-reactions that may accompany this process were studied using 31P NMR spectroscopy. These provided new insight into a possible mechanism involved in this transformation and constituted the basis for development of efficient methods for the preparation of nucleoside H-phosphonothioate and nucleoside H-phosphonodithioate monoesters using readily available H-phosphonate monoesters as starting materials.
NUCLEOSIDE H-PHOSPHONATES. X. STUDIES ON NUCLEOSIDE HYDROGENPHOSPHONOTHIOATE DIESTER SYNTHESIS
Stawinski, Jacek,Thelin, Mats,Zain, Rula
, p. 2157 - 2160 (2007/10/02)
Synthesis and chemical properties of nucleoside H-phosphonothioates are discussed in the context of possible application of these compounds as intermediates in the synthesis of oligonucleotide analogues.