It has been reported ( 1) that (+)-2,3-dimethylcyclopropane carboxylic acid
The Absolute Configuration of 1-Methylindane
✍ Scribed by Hans-Jürgen Hansen; Hans-Richard Sliwka; Werner Hug
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- German
- Weight
- 561 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
It is shown unequivocally by chemical correlations (cf. Schemes 1‐‐3) and Raman optical activity spectra (cf. Fig. 1 and 2) that the (R)‐configuration has to be attributed to (+)‐1‐methylindane ((+)‐1). This is in contradiction to an earlier assignment of the (R)‐configuration to (−)‐1[2] which was based on the (R)‐configuration of (+)‐indane‐1‐carboxylic acid (3) [11].
📜 SIMILAR VOLUMES
## Abstract Doubts that have recently been expressed [1] about the currently accepted (+)‐(__R__), (−)‐(__S__) [2] absolute configuration of indane‐1‐carboxylic acid appear to be unwarranted. __Our ORD. values for 1‐methylindane [12] are in error__.
DiTialon of chemioal PhJmfom, chomloal Xemewh Laborrtorieo, c.a.m.o., BOX 60 p.o., myton, vi0t0e, htrilia.