Cyclization-rearrangement of alkylstyrenes. 1. A. 1-Phenyl-1-pentene and homologs. B. A short synthesis of calamenene
β Scribed by Condon, Francis E.; West, David L.
- Book ID
- 127015395
- Publisher
- American Chemical Society
- Year
- 1980
- Tongue
- English
- Weight
- 613 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-3263
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The title compounds (VI), monomers for nucleic acid bases attached functional polymers, are synthesized for the first time from uracil or thymine in three steps using the Mitsunobu reaction of partially protected bases (III) with 2-chloroethanol as the key step. -(ZHOU,
## Abstract For mass spectrometric studies 1βphenylβ2βphenylβ1β^13^Cβetheneβ1β^13^C (transβstilbene) was synthesized from aceticβ1β^13^C acid and aceticβ2β^13^C acid via methylcyclohexeneβ1β^13^C and βΞ±β^13^C and tolueneβ1β^13^C and βΞ±β^13^C. No scrambling of the label was observed during the aroma