## Abstract The title compound **1** is a further example of an olefinic alcohol that undergoes ether formation under basic conditions **(→ 3)** although the double bond is not activated by an electron‐attracting group. This unusual reactivity is due to steric compression, which is increased in the
Mass spectrometric studies of the toxaphene components 2-exo,3-endo,5-exo,6-endo,8,8,10,10-octachloroborane (T2) and 2-exo,3-endo,5-exo,6-endo,8,8,9,10,10-nonachlorobornane (T12)
✍ Scribed by G. A. Stern; D. C. G. Muir; J. B. Westmore; W. D. Buchannon
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 706 KB
- Volume
- 22
- Category
- Article
- ISSN
- 1076-5174
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