✦ LIBER ✦

A Sulfitylation−Oxidation Protocol for the Preparation of Sulfates

✍ Scribed by Huibers, M.; Manuzi, Álvaro; Rutjes, Floris P. J. T.; van Delft, Floris L.

Book ID: 115478120
Publisher: American Chemical Society
Year: 2006
Tongue: English
Weight: 84 KB
Volume: 71
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo060404v

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Sulfitylation—Oxidation Protocol for t

A Sulfitylation—Oxidation Protocol for the Preparation of Sulfates.

✍ M. Huibers; Alvaro Manuzi; Floris P. J. T. Rutjes; Floris L. van Delft 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

A fusion method for the preparation of s

A fusion method for the preparation of steroid sulfates

✍ John P. Dusza; Joseph P. Joseph; Seymour Bernstein 📂 Article 📅 1985 🏛 Elsevier Science 🌐 English ⚖ 275 KB

A simple and highly effective oxidative

A simple and highly effective oxidative chlorination protocol for the preparation of arenesulfonyl chlorides

✍ Yu-Ming Pu; Alan Christesen; Yi-Yin Ku 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 506 KB

A greener synthetic protocol for the pre

A greener synthetic protocol for the preparation of carbodiimide

✍ Abdur Rezzak Ali; Harisadhan Ghosh; Bhisma K. Patel 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 209 KB

ChemInform Abstract: A Simple and Highly

ChemInform Abstract: A Simple and Highly Effective Oxidative Chlorination Protocol for the Preparation of Arenesulfonyl Chlorides.

✍ Yu-Ming Pu; Alan Christesen; Yi-Yin Ku 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

On the preparation of carbohydrate sulfa

On the preparation of carbohydrate sulfates by displacement of trifluoromethanesulfonates

✍ John A. Hyatt; James L. Little 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 178 KB

A recent paper by Latif et.al.' described the reaction of certain carbohydrate trifluoromethanesulfonates (triflates) with tetrabutylammonium hydrogensulfate in acetonitrile solution to produce hydrogensulfates. In a particular example, benzyl 2,3-anhydro-CO-(trifluoromethanesulfonyl)-cr-D-lyxopyran