WebNov 11, 2024 · First, EDA was mono-protected using Boc anhydride, followed by Fmoc protection on the other primary amine of EDA. Finally, Boc was removed under acidic conditions to yield the Fmoc–EDA as TFA salt. However, the following step of alkylation with benzyl bromoacetate failed because of the instability of the free base on the intermediate. WebBoc Protecting Group Before the Fmoc group became popular, the t-Boc group was commonly used for protecting the terminal amine of the peptide, requiring the use of …
BOC Protection and Deprotection - J&K Scientific LLC
WebWith triethylamine In water; acetone at 20℃; for 4 h; ... In another flask BOC-anhydride was taken into 1,4-dioxane (25 ml), cooled to 0-5° C., added to the above reaction mixture and stirred the reaction mixture overnight. Extracted with ethylacetate (150 ml.x.1). The aqueous layer acidified with 1:1 aqueous. Hydrochloric acid up to pH 2 ... WebBoc anhydride, Di-tert-butyl pyrocarbonate Linear Formula: [ (CH3)3COCO]2O CAS Number: 24424-99-5 Molecular Weight: 218.25 Beilstein: 1911173 Número de EC: 246-240-1 Número MDL: MFCD00008805 ID de la sustancia en PubChem: 24852315 NACRES: NA.22 Recommended Products Sigma-Aldrich 34660 Di-tert-butyl dicarbonate ≥98.0% (GC) megabad keuco edition 11
Boc-Protected Amino Groups - Organic Chemistry
WebCode: B 3080. (For eg. B 1615-0108) Description. Since this compound can be regarded formally as the acid anhydride derived from a tert-butoxycarbonyl (Boc) group, it is … WebThe invention relates to propionic acids, propionic acid esters, and related compounds, pharmaceutical compositions containing these compounds, and methods of using these compounds for the treatment of various diseases or conditions, including but not limited to diseases and/or conditions of Central Nervous System (CNS). Webtriethylamine, with the imine 3 gave 5 [mp 74–76 °C, [ a]25D +1.6 (CH2Cl2, c 1.0)] in 85% yield. In each case a single diastereoisomer was produced as judged by 1H NMR analysis of the crude reaction products. The relative cis-disposition of the substituents at the C3 and the C4 positions of the b-lactam ring megabad widerrufsformular