✦ LIBER ✦

Synthesis of phosphotyrosine-containing peptides using bis-(2, 2, 2-trichloro)ethyl groups for phosphate protection

✍ Scribed by PAQUET, ALENKA ;BLACKWELL, BARBARA ;JOHNS, MICHAEL ;NIKIFORUK, JOHN

Book ID: 110893630
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 563 KB
Volume: 50
Category: Article
ISSN: 1397-002X
DOI: 10.1111/j.1399-3011.1997.tb01467.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

N,N′-Dialkyldiamide-type phosphate prote

N,N′-Dialkyldiamide-type phosphate protecting groups for Fmoc synthesis of phosphotyrosine-containing peptides

✍ Masaaki Ueki; Jun Tachibana; Yusuke Ishii; Jin Okumura; Mitsutaka Goto 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 255 KB

Further studies on the use of 2,2,2-tric

Further studies on the use of 2,2,2-trichloroethyl groups for phosphate protection in phosphoserine peptide synthesis

✍ PAQUET, ALENKA 📂 Article 📅 2009 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 414 KB

ChemInform Abstract: N,N′-Dialkyldiamide

ChemInform Abstract: N,N′-Dialkyldiamide-Type Phosphate Protecting Groups for Fmoc Synthesis of Phosphotyrosine-Containing Peptides: Optimization of the Alkyl Group.

✍ M. UEKI; M. GOTO; J. OKUMURA; Y. ISHII 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 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

A novel phosphate protection for oligonu

A novel phosphate protection for oligonucleotide synthesis: the 2-[(1-naphthyl)carbamoyloxy]ethyl (NCE) group

✍ Andrei P Guzaev; Muthiah Manoharan 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 104 KB

The utility of the 2-(arylcarbamoyloxy)ethyl group for protection of internucleosidic phosphate linkages in oligonucleotide synthesis was studied. Of the three protecting groups tested, the 2-[(1-naphthyl)carbamoyloxy]ethyl demonstrated high coupling yields, favorable deprotection kinetics and the h

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

N,N-Diisopropyl-bis[2-(trimethylsilyl)et

N,N-Diisopropyl-bis[2-(trimethylsilyl)ethyl]phosphoramidite. An attractive phosphitylating agent compatible with the Fmoc/t-butyl strategy for the synthesis of phosphotyrosine containing peptides

✍ Hann-Guang Chao; Michael S. Bernatowicz; Clifford E. Klimas; Gary R. Matsueda 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 256 KB