𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A new synthesis of secondary allylic aliphatic and aromatic amines

✍ Scribed by Andreas Spaltenstein; Philip A. Carpino; Paul B. Hopkins

Book ID
104218077
Publisher
Elsevier Science
Year
1986
Tongue
French
Weight
274 KB
Volume
27
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Synthesis of New Ox
ChemInform Abstract: Synthesis of New Oxamide Derivatives of D-Glucosamine and Aliphatic or Aromatic Amines.
✍ Andrzej Temeriusz; Boguslawa Piekarska-Bartoszewicz; Magdalena Rowinska πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 2 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 β€œFull Text” option. The original article is trackable v

Synthesis and properties of aromatic sec
Synthesis and properties of aromatic secondary amine-blocked isocyanates
✍ A. Sultan Nasar; S. Subramani; Ganga Radhakrishnan πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 151 KB πŸ‘ 2 views

N-Methylaniline-, diphenylamine-, and N-phenylnaphthylamine-blocked toluene diisocyanates (TDI) were prepared and characterized by IR, NMR spectroscopy, and nitrogen content analyses. The structure-property relationship of these adducts was established by reacting with hydroxyl-terminated polybutadi

Ruthenium-Catalyzed Synthesis of Seconda
Ruthenium-Catalyzed Synthesis of Secondary Alkylamines: Selective Alkylation with Aliphatic Amines
✍ Sebastian BΓ€hn; Dirk Hollmann; Annegret Tillack; Matthias Beller πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 184 KB πŸ‘ 1 views

## Abstract The chemoselective __N__‐alkylation of __tert__‐alkylamines applying aliphatic amines is described for the first time. In the presence of the Shvo catalyst **1**, __tert__‐octylamine **4** and 1‐adamantylamine **5** are alkylated using primary, secondary, and even tertiary amines to giv