Topic
Norbornadiene
About: Norbornadiene is a research topic. Over the lifetime, 2389 publications have been published within this topic receiving 38603 citations.
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TL;DR: Adipinato(bicyclo[2.2.1]-hepta-2,5-diene)bis(pyridine)dicopper(I) pyridine was obtained by the reaction of adipinatodicopper (I) with bicyclo[1.2] hepta 2,5,diene (BH 2.5) and its structure determined by an X-ray diffraction study as mentioned in this paper.
4 citations
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07 Sep 1978
TL;DR: In this article, the ring-opening polymerization of norbornene or norbornadiene derivative is conducted in the presence of a specific catalyst, and it is shown that the ring opening polymerization is reversible.
Abstract: PURPOSE:The ring-opening polymerization of norbornene or norbornadiene derivative is conducted in the presence of a specific catalyst.
4 citations
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TL;DR: Dehydration of the formyl acid with acetic anhydride in benzene at 80 °C generates the quinonoid pyrone 4 which can be trapped with norbornadiene, N-phenylmaleimide and enol silyl ethers.
Abstract: Dehydration of the formyl acid 3(R = H) with acetic anhydride in benzene at 80 °C generates the quinonoid pyrone 4 which can be trapped with norbornadiene, N-phenylmaleimide and enol silyl ethers; the adduct 6(R = Me, P = TES) and its 9-epimer 10 from 2-(triethylsilyloxy)propene are readily transformed into (±)-auramycinone 2(R = Me) whilst those [6(R = vinyl, P = TES) and its 9-epimer] from 2-(triethylsilyloxy)buta-1,3-diene are readily converted into the methyl ethers 24, 25, 33 and 34 of which 24, 33 and 34 are known to be readily converted into (±)-aklavinone 2(R = Et).
4 citations
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TL;DR: Norbornadiene tetramers exo-trans-exo-Trans-Exo -TransExo-End -Dodecacyclo [14.9.1.
4 citations
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4 citations