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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

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✦ 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].


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✍ James H. Brewster 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 German ⚖ 441 KB

## 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__.