WebReagent for SEM protection. Procedure excerpt:. . . the SM (8.1 g, 33.1 mmol) in DMF (165 mL) was cooled 0 C and NaH (60% in mineral oil, 1.98 g, 49.6 mmol) was added. After 30 min, SEM-Cl (7.02 mL, 39.7 mmol) was added . . . ... (Trimethylsilyl)ethoxymethyl chloride ... WebAcetal protection of a ketone with ethylene glycol during reduction of an ester, vs. reduction to a diol when unprotected. A protecting group or protective group is introduced into a …
Protecting Groups Handout A - University of Houston
WebProtection of Amino Groups. 1-Alkyl-3-methylimidazolium cation based ionic liquids efficiently catalyze N-tert-butyloxycarbonylation of amines with excellent chemoselectivity.The catalytic role of the ionic liquid is envisaged as electrophilic activation of di-tert-butyl dicarbonate (Boc 2 O) through bifurcated hydrogen bond formation with the … WebStability Protection of Amino Groups The reaction of aliphatic and aromatic secondary and tertiary N -tritylamines with lithium powder and a catalytic amount of naphthalene led to reductive detritylation affording the corresponding amines in good yields. The trityl group could selectively be removed in the presence of an allyl or a benzyl group. tbk studio
(PDF) An Efficient Deprotection of N -Trimethylsilylethoxymethyl (SEM
WebA simple and efficient method has been developed for chemoselective deprotection of phenolic methoxymethyl (MOM) ethers at room temperature using silica-supported sodium hydrogen sulfate as a heterogeneous catalyst. C. Ramesh, N. Ravindranath, B. Das, J. Org. Chem., 2003 , 68, 7101-7103. http://www.commonorganicchemistry.com/Rxn_Pages/SEM_Protection/SEM_Protection_HCl.htm http://commonorganicchemistry.com/Common_Reagents/2-(Trimethylsilyl)ethoxymethyl_Chloride/2-(Trimethylsilyl)ethoxymethyl_Chloride.htm tbk stainless steel