𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A [1,2] and a [1,4] shift in a Wittig thioether rearrangement. Isolation of a [1.1](2,8)naphthalenophane tautomer

✍ Scribed by Gleiter, Rolf; Schaaff, Hans Peter; Huber-Patz, Ursula; Rodewald, Hans; Goetzmann, Wolfgang; Irngartinger, Hermann


Book ID
127277087
Publisher
American Chemical Society
Year
1987
Tongue
English
Weight
466 KB
Volume
52
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


1,2-Shift of a Carboxyl Group in a Wagne
✍ Daniel Berner; D. Philip Cox; Hans Dahn πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 German βš– 535 KB

## Abstract On treatment with HSO~3~F in SO~2~C1F at 0Β°, 3‐hydroxy‐2,2‐dimethyl‐3‐phenyl‐propionic acid (**1a**) is transformed into 2‐phenyl‐3‐methyl‐2‐butenoic acid (**2a**) (isolated yield: 40–44%). Using monolabelled [3‐^13^C]‐**1a** (**1a**\*) and doubly labelled [1,3‐^13^C~2~]‐**1a** (**1a**\

Stereochemistry of the 1,2-Wittig rearra
✍ Stuart L. Schreiber; Mark T. Goulet πŸ“‚ Article πŸ“… 1987 πŸ› Elsevier Science 🌐 French βš– 259 KB

The [1,2] Wittig rearrangement of P-alkoxyalkyl ally1 ethers has been studied and found to provide syn-1,3-diol derivatives in 14-32% yield and with useful levels of diastereoselection. The rearrangement of a-metalated ethers (Wittig rearrangement) has been of interest to investigators since its di

Intramolecular Electron Transfer between
✍ Alexander R. Wartini; Heinz A. Staab; Franz A. Neugebauer πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 887 KB

Various radical cations, in which two terminal 1,4dimethoxybenzene units are anellated to [2.2]paracyclophane (2b and anthracene bridges (5 β€’+ ), have been studied by ESR and ENDOR spectroscopy. In the syn-and anti-naphthalenophane radical cations 2b β€’+ and 3b β€’+ the delocalization of the unpaired