Selective deprotection of trialkylsilyl ethers using fluorosilicic acid

…, DK Hill, SJ Shimshock, RE Waltermire…

Index: Pilcher, Anthony S.; Hill, David K.; Shimshock, Stephen J.; Waltermire, Robert E.; DeShong, Philip Journal of Organic Chemistry, 1992 , vol. 57, # 8 p. 2492 - 2495

Full Text: HTML

Citation Number: 70

Abstract

Conclusions In conclusion, we have described a general, new and simple procedure for the synthesis of 3'-carbonates of pyrimidine and purine 2'-deoxynucleosides. In this me-thod, no previous protection of the primary hydroxyl group is necessary, as has been traditionally described for preparation of these compounds.

Related Articles:

Improved protocols for the selective deprotection of trialkylsilyl ethers using fluorosilicic acid

[Pilcher, Anthony S.; DeShong, Philip Journal of Organic Chemistry, 1993 , vol. 58, # 19 p. 5130 - 5134]

Fluorous TBAF: a convenient and selective reagent for fluoride-mediated deprotections

[Fustero, Santos; Sancho, Amador Garcia; Acena, Jose Luis; Sanz-Cervera, Juan F. Journal of Organic Chemistry, 2009 , vol. 74, # 16 p. 6398 - 6401]

More Articles...