✦ LIBER ✦

A New Protecting Group “3′,5′-O-Sulfinyl” for Xylo-Nucleosides. A Simple and Efficient Synthesis of 3′-Amino-3′-deoxyadenosine (a Puromycin Intermediate), 2,2′-Anhydro-pyrimidine Nucleosides and 2′,3′-Anhydro-adenosine.

✍ Scribed by Ken-ichi Takatsuki; Makoto Yamamoto; Sumito Ohgushi; Shigeo Kohmoto; Keiki Kishikawa; Haruhiro Yamashita

Publisher: John Wiley and Sons
Year: 2004
Weight: 120 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200415193

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Simple and Efficient Synthesis of Puro

A Simple and Efficient Synthesis of Puromycin, 2,2′-Anhydro-pyrimidine Nucleosides, Cytidines and 2′,3′-Anhydroadenosine from 3′,5′-O-Sulfinyl xylo-Nucleosides

✍ Ken-ichi Takatsuki; Sumito Ohgushi; Shigeo Kohmoto; Keiki Kishikawa; Makoto Yama 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

Synthesis of 2-Amino-2,4-anhydro-3-O-(2-

Synthesis of 2-Amino-2,4-anhydro-3-O-(2-tetrahydropyranyl)psicofuranose: A Versatile Intermediate for S-Type Locked Nucleosides.

✍ Chamakura V. N. S. Varaprasad; Kanda S. Ramasamy; Zhi Hong 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 9 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.