The 4-oxopentyl group as a labile phosphate/thiophosphate protecting group for synthetic oligodeoxyribonucleotides

ChemInform Abstract: The 4-Oxopentyl Gro

ChemInform Abstract: The 4-Oxopentyl Group as a Labile Phosphate/Thiophosphate Protecting Group for Synthetic Oligodeoxyribonucleotides.

✍ Andrzej Wilk; Marcin K. Chmielewski; Andrzej Grajkowski; Lawrence R. Phillips; S 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Allyl Group as a Pr

ChemInform Abstract: Allyl Group as a Protecting Group for Internucleotide Phosphate and Thiophosphate Linkages in Oligonucleotide Synthesis: Facile Oxidation and Deprotection Conditions.

✍ Muthiah Manoharan; Yixin Lu; Martin D. Casper; George Just 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

The 2,2,2,-Trichloroethyl Group as a Pro

The 2,2,2,-Trichloroethyl Group as a Protecting Group for Phosphate in the Synthesis of Mononucletides

✍ Dr. F. Eckstein 📂 Article 📅 1965 🏛 John Wiley and Sons 🌐 English ⚖ 124 KB 👁 2 views

The 2-(acetoxymethyl)benzoyl (AMB) group

The 2-(acetoxymethyl)benzoyl (AMB) group as a new base-protecting group, designed for the protection of (phosphate) modified oligonucleotides.

✍ W.H.A. Kuijpers; J. Huskens; C.A.A. van Boeckel 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 223 KB

1,1,1,3,3,3-Hexafluoro-2-propyl group as

1,1,1,3,3,3-Hexafluoro-2-propyl group as a new phosphate protecting group for oligoribonucleotide synthesis in the phosphotriester approach

✍ Shunichi Yamakage; Masayo Fujii; Hiroshi Takaku; Masaru Uemura 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 508 KB

The 1,1,1,3,3,3-Hexafluoro-2-propyl group can be used as a new class of phosphate protecting group for the protecting group of internucleotidic bonds in the oligonucleotide synthesis by the phosphotriester approach . This protecting group is removed easily by treatment with 0 .3 M N 1 ,N 1 ,N 3 ,N''

The 4-nitrobenzenesulfonyl group as a co

The 4-nitrobenzenesulfonyl group as a convenient N-protecting group for iminosugars—synthesis of oligosaccharide inhibitors of heparanase

✍ Zsuzsánna Csíki; Péter Fügedi 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 315 KB