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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (or DDQ) is the chemical reagent with formula C 6 Cl 2 (CN) 2 O 2. This oxidant is useful for the dehydrogenation of alcohols, [3] phenols, [4] and steroid ketones. [5] DDQ decomposes in water, but is stable in aqueous mineral acid. [6]
The use of protective groups is pervasive but not without criticism. [103] In practical terms their use adds two steps (protection-deprotection sequence) to a synthesis, either or both of which can dramatically lower chemical yield. Crucially, added complexity impedes the use of synthetic total synthesis in drug discovery.
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R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry , benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5 . Benzyl features a benzene ring ( C 6 H 6 ) attached to a methylene group ( −CH 2 − ).
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containing entries that are not themselves sections. Also, use {{R to anchor}} where appropriate. For a redirect to an article section about the subject use the {{R to section}} rcat instead. For a redirect from a topic to a related list and not to an entry on that list, use {{R from list topic}} instead.
Use in artificial nucleotide synthesis [ edit ] 1- O -Acetyl-2,3,5-tri- O -benzoyl-β- D -ribofuranose is further reacted with trimethylsilyl trifluoromethanesulfonate (TMSOTf) under the silyl-Hilbert–Johnson reaction and deprotected by an acid or base to form a pure artificial nucleotide.
The use of Fmoc as a temporary protecting group for amine at the N-terminus in solid phase synthesis is very widespread for Fmoc/tBu approach, because its removal with piperidine does not disturb the acid-labile linker between the peptide and the resin. [7]