✦ LIBER ✦

A Convenient Preparation of Tetrahydrofuran-Based Diamines.

✍ Scribed by Gaifa Lai

Publisher: John Wiley and Sons
Year: 2004
Weight: 21 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200442123

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Convenient Preparation of a Series of

A Convenient Preparation of a Series of 2-Aryl-Substituted Imidazolidines Through Diamine Transfer Reaction.

✍ Donghong Li; Yongbin Zhang; Chizhong Xia; Wei Guo 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 15 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

A Convenient Preparation of Isothiocyana

A Convenient Preparation of Isothiocyanates

✍ Dr. R. Gottfried 📂 Article 📅 1966 🏛 John Wiley and Sons 🌐 English ⚖ 249 KB 👁 1 views

mixture with heptane, from which it is crystallized a t -80 "C. The yield was 27 % calculated on the total amount of starting material, and 54 "/, on the amount consumed. CzH5Cp2ZrCI is a crystalline, intensely yellow, diamagnetic compound [xg = -(0.44 & 0.04) x 10-6 E.M.U./g], which is decomposed

ChemInform Abstract: Convenient Preparat

ChemInform Abstract: Convenient Preparation of Chiral trans-9,10-Dihydrophenanthrene-9,10-diamine.

✍ Shuang-Zheng Lin; Tian-Pa You 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

A Convenient Preparation of Xanthene Dye

A Convenient Preparation of Xanthene Dyes.

✍ Youjun Yang; Jorge O. Escobedo; Alexander Wong; Corin M. Schowalter; Michael C. 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 23 KB

Brønsted Basicities of Diamines in the G

Brønsted Basicities of Diamines in the Gas Phase, Acetonitrile, and Tetrahydrofuran

✍ Eva-Ingrid Rõõm; Agnes Kütt; Ivari Kaljurand; Ivar Koppel; Ivo Leito; Ilmar A. K 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB

A convenient preparation of 18O-dimethyl

A convenient preparation of 18O-dimethylformamide

✍ R. Rao Koganty; George A. Digenis 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 French ⚖ 121 KB 👁 1 views

## Abstract A method is described by which ^18^O‐DMF can be prepared conveniently and in very high yields (∼ 90%) by reacting at room temperature an equimolar quantity of benzoyl chloride, DMF and ^18^O‐labelled water.