Description
Additional Properties
Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents Application Review of synthetic utility.1 Review on organosilane protecting groups.2 Reagent for protection of 3',5' hydroxy nucleosides.3,4 Key review in natural products synthesis.5 Protects the four equatorial hydroxyls of inositol in a single step.6 Fieser F&F: Vol. 16, p 125. Reference 1. Handbook of Reagents for Organic Synthesis, Reagents for Silicon-Mediated Organic Synthesis, Fuchs, P. L. Ed., John Wiley and Sons, Ltd., 2011, p. 230-233. 2. Larson, G. L. “Silicon-Based Blocking Agents” Gelest, Inc. 2014. 3. Kanaya, E. N. et al. Biochemistry 1987, 26, 7159. 4. Markiewicz, W. J. Chem. Res. 1979, 24. 5. Ziegler, T. et al. Trends Org. Chem. 1997, 6, 91. 6. Martin-Lomas, M. et al. Eur. J. Org. Chem. 2000, 1539. Safety
Packaging Under Nitrogen Bridging Silicon-Based Blocking Agent Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure. Tetraisopropyldichlo
rodisiloxane; Dichlorotetraisoprop
yldisiloxane; 1,3-Dichloro-1,1,3,3
-tetraisopropyldisil
oxane; TIPDS
Highly useful for protection of 3’,5’- dihydroxynucleosides
Protects 1,2-diequatorial diols
Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
