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Chlorophosphoramidite derivatives

Chlorophosphoramidite Derivatives Useful in the Synthesis of Deoxyribonucleoside Phosphoramidites... [Pg.41]

Chloro-1,3,2-oxazaphospholanc (chlorophosphoramidite) 43 derived from (IR, 25)-(-)-cphedrine 42 was prepared for the first time as early as 1977 by its reaction with phosphorus trichloride (Scheme 15) [32, 33], Later, similar procedures were reported for its isolation as a single epimer which, on the basis of spectroscopic and derivatisation studies, has been assigned configuration [34-36],... [Pg.111]

In continuation of work in Just s laboratory on the diastereoselective synthesis of dinucleoside phosphorothioates, the chlorophosphoramidite 219 (for the synthesis of the aminoalcohol see Chapter 14) was converted as indicated in Scheme 8 into the Sp-isomer 220, in a 6 1 ratio with the diastereomer, and this ratio could be improved by the use of a more hindered base in step ii. The auxiliary 221, derived from L-tryptophan, has also been used. When 221 was treated sequentially with 5 -0-Tbdms-thymidine, 3 -0-Tbdms-thymidine and Beaucage s reagent, a phosphorothioate triester was produced. The auxiliary could be removed as the aminomethyl compound by treatment with ammonia, to give the i p-isomer of 220, in 40 1 excess. ... [Pg.278]


See other pages where Chlorophosphoramidite derivatives is mentioned: [Pg.112]    [Pg.287]    [Pg.177]    [Pg.203]    [Pg.64]   
See also in sourсe #XX -- [ Pg.41 ]




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