## Abstract 2,3‐Dimethylene‐2,3‐dihydrothiophene (1), the thiophene analog of o‐xylylene (o‐quinodimethane), was generated __in situ__ from the (trialkylammoniomethyl)‐(trimethylsilylmethyl)thiophene iodides 4 or 5 by fluoride‐induced 1,4 climination, and was trapped by [4 + 2] cycloadditions with
Synthesis and cycloaddition reaction of 2,3-dimethylene-7-isopropylidenebenzonorborene
✍ Scribed by Tadashi Sasaki; Takashi Manabe; Kenji Hayakawa
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 221 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Synthesis of 2,3-dimethylene-7-isopropylidenebenzonorbornene (2) and its cycloaddition reactions with dichloroketene and dienophiles are described. Recently, interesting stereoselectivities in cycloaddition reactions of molecules containing proximal n-bonds have been reported, and the factors controlling them have been extensively explored.'
We have already reported that 7-isopropylidenebenzonorbornadiene 1 shows remarkable
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Dimethylenecyclopolyenes of type 1. are an interesting class of compounds. The n=l member of this class is 3,6-dimethylene-1,4-cyclohexadiene 2 which is an important intermediate for [2.2]paracyclophane. 1 -Of two possible dimethylenecyclooctatrienes, 7,8-dimethylene-1,3,5-cyclooctatriene 2 was sy
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract The regioselective synthesis of dimethyl 1,3,5‐cyloheptatriene‐1,2‐dicarboxylate (4) was achieved by a ring expansion method, starting from dimethyl 1,3‐cyclohexadiene‐2,3‐dicarboxylate (5). The title compound 3 was obtained as an air‐sensitive oil by zinc‐copper reduction of 1,2‐bis(br
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