thiourea and carbon-tetrabromide

thiourea has been researched along with carbon-tetrabromide* in 1 studies

Other Studies

1 other study(ies) available for thiourea and carbon-tetrabromide

Article	Year
Allyl group as a protecting group for internucleotide phosphate and thiophosphate linkages in oligonucleotide synthesis: facile oxidation and deprotection conditions. Organic letters, 2000, Feb-10, Volume: 2, Issue:3 [reaction: see text] The allyl group, which serves as a protecting group for an internucleotide bond for both phosphates and phosphorothioates, can be easily removed by good nucleophiles under weakly basic or neutral conditions. For a practical synthesis on solid support, camphorsulfonyloxaziridine was used as the oxidizing agent for synthesizing DNA, while the Beaucage reagent was used for preparing phosphorothioate oligomers. Both types of oligonucleotides were easily deprotected by concentrated ammonium hydroxide containing 2% mercaptoethanol. Topics: Acetylene; Benzofurans; Catalysis; Combinatorial Chemistry Techniques; Hydrocarbons, Brominated; Palladium; Thiourea	2000

Article

Year

Allyl group as a protecting group for internucleotide phosphate and thiophosphate linkages in oligonucleotide synthesis: facile oxidation and deprotection conditions.

Organic letters, 2000, Feb-10, Volume: 2, Issue:3

[reaction: see text] The allyl group, which serves as a protecting group for an internucleotide bond for both phosphates and phosphorothioates, can be easily removed by good nucleophiles under weakly basic or neutral conditions. For a practical synthesis on solid support, camphorsulfonyloxaziridine was used as the oxidizing agent for synthesizing DNA, while the Beaucage reagent was used for preparing phosphorothioate oligomers. Both types of oligonucleotides were easily deprotected by concentrated ammonium hydroxide containing 2% mercaptoethanol.

Topics: Acetylene; Benzofurans; Catalysis; Combinatorial Chemistry Techniques; Hydrocarbons, Brominated; Palladium; Thiourea

2000