A novel reaction of 2,3-dichloro-5,6-dicyanobenzoquinone with heptafulvenes. Formation of 1,2-dicyanoazulenes
✍ Scribed by Shigeyasu Kuroda; Makoto Funamizu; Yoshio Kitahara; Toyonobu Asao
- Book ID
- 104213805
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 107 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
2,3-Dichloro-5,6-dicyanobenzoquinone (004) is well known useful oxidizing reagent in organic synthesis and has powerful ability in complex formation with unsaturated compounds.L However, only one report on the cycloaddition of DDQ has appeared,3 in spite of p-benzoquinone
📜 SIMILAR VOLUMES
Paulownin and gmelinol react with DDQ to give 4-pyrone derivatives. Gummadiol reacts under the same conditions to give a pyrone aldehyde and an unsaturated y-lactone. 2,3-Dichloro-5,6-dicyanobenzoquinone (DDQ) has been previously shown to react with lignans of the monoarylidene-butyrolactone and ary
## Abstract The dehydrogenation of 1,4‐cyclohexadiene (**1**) __cis__‐3,6‐dimethyl‐1,4‐cyclohexadiene (**2**) and __trans__‐3,6‐dimethyl‐1,4‐cyclohexadiene (**3**) with triphenylmethylfluoroborate in acetonitrile or 2,3‐dichloro‐5,6‐dicyanobenzoquinone (DDQ) proceeds in the same reactivity sequence