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・ 4'-demethylrebeccamycin synthase
・ 4'-Fluoro-α-pyrrolidinooctanophenone
・ 4'-Fluoro-α-pyrrolidinopentiophenone
・ 4'-Hydroxyisoflavone methyltransferase
・ 4'-Methoxy-α-pyrrolidinopentiophenone
・ 4'-Methoxy-α-pyrrolidinopropiophenone
・ 4'-methoxyisoflavone 2'-hydroxylase
・ 4'-Methyl-α-pyrrolidinobutiophenone
・ 4'-Methyl-α-pyrrolidinohexiophenone
・ 4'-Methyl-α-pyrrolidinopropiophenone
・ 4'-O-glucoside
・ 4'-phosphopantetheinyl transferase
・ 4+1 architectural view model
・ 4+1 Ensemble
・ 4+3 cycloaddition
4+4 Photocycloaddition
・ 4, 3, 2, 1
・ 4, 3, 2, 1 (k-os song)
・ 4, 3, 2, 1 (LL Cool J song)
・ 4, 5 and 6
・ 4, 5, 6
・ 4,000 Weeks' Holiday
・ 4,16-Androstadien-3β-ol
・ 4,21-Dehydrogeissoschizine
・ 4,4'-Azobis(4-cyanopentanoic acid)
・ 4,4'-Biphenol
・ 4,4'-Bipyridine
・ 4,4'-Diapophytoene desaturase
・ 4,4'-Diapophytoene synthase
・ 4,4'-Dichlorobenzophenone


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4+4 Photocycloaddition : ウィキペディア英語版
4+4 Photocycloaddition

The () Photocycloaddition is a cycloaddition reaction in which two unsaturated molecules connect via four atoms from each molecule (hence "4 + 4") to create an eight-membered ring. As a photochemical reaction, it is promoted by some form of light, as opposed to a thermal process.
== Introduction ==

The earliest example of a () photocycloaddition was the photodimerization of anthracene, discovered in 1936. This reaction has remained one of the most reliable photocycloadditions and is the basis of continuing investigation.
Other polycyclic aromatics undergo anthracene-like photocycloaddition, such as acridizinium salts. Biologically active natural products include pleuromutilin, kalmanol, crenulide, and longipenol.
() photocycloaddition approaches to the creation of cyclooctanoid systems offer several appealing features, including convergent assembly of the eight-membered ring from two relatively simpler four-carbon fragments, formation of two new carbon-carbon bonds, and the potential for introduction of up to four new stereocenters in one step.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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