Aryl H-phosphonates. Part IV. A new method for internucleotide bond formation based on transesterification of aryl nucleoside H-phosphonate diesters

DOI: 10.1016/0040-4039(96)00846-5

Source and publish data:

Tetrahedron Letters p. 4561 - 4564 (1996)

Update date:2022-08-04

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Authors:

Cieslak, Jacek

Sobkowski, Michal

Kraszewski, Adam

Stawinski, Jacek

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Article abstract of DOI:10.1016/0040-4039(96)00846-5

Under mild reaction conditions nucleoside aryl H-phosphonate diesters undergo fast and efficient transesterification with suitably protected nucleosides, affording dinucleoside (3'-5') H-phosphonate diesters.

Full text of DOI:10.1016/0040-4039(96)00846-5

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Article Doi

Aryl H-phosphonates. Part IV. A new method for internucleotide bond formation based on transesterification of aryl nucleoside H-phosphonate diesters

DOI: 10.1016/0040-4039(96)00846-5

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(96)00846-5

Full text of DOI:10.1016/0040-4039(96)00846-5

Products guided by the article

R&D Labs maybe for 180475-93-8

Relevant to this article

Complexes of trivalent phosphorus derivatives. III. Metal carbonyl complexes of 9-phenyl-9-phosphabicyclo[4.2.1]nonatriene

The derivatives of the 2a,4a-diazacyclopenta[c,d]azulene

New cyclization mechanism for squalene: A ring-expansion step for the five-membered C-ring intermediate in hopene biosynthesis

Bile acid-piperazine diamides: Novel steroidal templates in syntheses of supramolecular hosts: Isomeric pyridine-n-carboxy containing dimers and a cholaphane

First total syntheses of oresbiusins A and B, their antipodes, and racemates: Configuration revision and anti-HIV activity

1,4-asymmetric induction in the chromium(II)- and indium-mediated coupling of allyl bromides to aldehydes