✦ LIBER ✦

N-Trimethylsilyl-substituted Sulfurous Diamides and Monoimides; N-Alkyl-N′-phenyl(sulfur diimides)

✍ Scribed by Dr. O. J. Scherer; P. Hornig

Publisher: John Wiley and Sons
Year: 1966
Tongue: English
Weight: 210 KB
Volume: 5
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.196607291

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The First N-Alkyl-N′-polyfluorohetaryl S

The First N-Alkyl-N′-polyfluorohetaryl Sulfur Diimide.

✍ Enno Lork; Ruediger Mews; Makhmut M. Shakirov; Paul G. Watson; Andrey V. Zibarev 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

N-Trimethylsilyl-substituierte Schweflig

N-Trimethylsilyl-substituierte Schwefligsäure-diamide und -imide sowie N-Alkyl-N′-phenyl-schwefeldiimide

✍ Dr. O. J. Scherer; P. Hornig 📂 Article 📅 1966 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB 👁 1 views

Reactive Derivatives of Aliphatic N-Sulf

Reactive Derivatives of Aliphatic N-Sulfinylamines—Alkylation of N-Sulfinylalkylamines and Bis (tert-butyl)-sulfur Diimide

✍ Prof. Dr. Günter Kresze; Dipl.-Chem. Michael Rössert 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 110 KB 👁 1 views

ChemInform Abstract: Comparative Spectro

ChemInform Abstract: Comparative Spectroscopic and Mechanistic Studies of Some Trimethylsilyl N-Alkyl-N-phenyl-carbamates

✍ Roland Szalay; Dezso Knausz; Janos Rohonczy; Pal Sohar 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

Time-Resolved Spectroscopy of Sulfur- an

Time-Resolved Spectroscopy of Sulfur- and Carboxy-Substituted N-Alkylphthalimides

✍ Helmut Görner; Axel G. Griesbeck; Thomas Heinrich; Wolfgang Kramer; Michael Oelg 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 189 KB 👁 1 views

Solvolysis of N,N-dimethylthiocarbamoyl

Solvolysis of N,N-dimethylthiocarbamoyl chloride: effect of sulfur-for-oxygen substitution upon kinetics and product partitioning

✍ Dennis N. Kevill; Todd M. Rudolph; Malcolm J. D'Souza 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 58 KB

A study of the solvolyses of N,N-dimethylcarbamoyl chloride (1) was extended to the solvolyses of N,N-dimethylthiocarbamoyl chloride (2). The specific rates of solvolysis of 2 at 0.0 °C are two to three orders of magnitude greater than those for 1. Analysis of the data using the extended Grunwald-Wi