Conjugation Chemistry/Click Chemistry (9656)
Click chemistry is a synthetic approach proposed by chemist K. Barry Sharpless 21 years ago. Its primary objective is to efficiently and reliably achieve the chemical synthesis of diverse molecules by connecting small building blocks. This concept places special emphasis on creating new combinatorial chemistry techniques centered on carbon-heteroatom bond (CXC) formation, leveraging these reactions (known as click reactions) to achieve molecular diversity in a straightforward and efficient manner.
tert-butyl 3-ethynylazepane-1-carboxylate
(2R,3S,4R)-2-(hydroxymethyl)-3,4-dihydro-2H-pyran-3,4-diol
(R,E)-cyclooct-4-en-1-yl (4-nitrophenyl) carbonate
(2S,3R,4S,5S,6S)-6-(methoxycarbonyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate
1-(chloromethyl)-4-ethynylbenzene
tert-butyl prop-2-yn-1-ylcarbamate
tert-butyl 4-ethynyl-[1,4'-bipiperidine]-1'-carboxylate
4-ethynylpiperidine hydrochloride
(prop-2-yn-1-yloxy)benzene
3-(4-((bis((1-(tert-butyl)-1H-1,2,3-triazol-4-yl)methyl)amino)methyl)-1H-1,2,3-triazol-1-yl)propan-1-ol
Oleic-DBCO
4-(cyclopropylethynyl)benzoic acid
1-(but-3-yn-1-yl)azepane
3-(3,5-dichlorophenyl)propiolic acid
4-ethynyl-1H-pyrazole
5-ethynyl-1H-indazole
3-(4-methoxyphenyl)propiolic acid
(3aR,5S,6R,6aR)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol
2-ethynylpyridine
Dibenzocyclooctyne-PEG4 maleimide
4,4,5,5-tetramethyl-2-(prop-1-yn-1-yl)-1,3,2-dioxaborolane
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(nonyloxy)tetrahydro-2H-pyran-3,4,5-triol
2-hydroxy-5-(phenylethynyl)benzoic acid
4-ethynyl-2-oxabicyclo[2.2.2]octane
4-ethynyltetrahydro-2H-pyran
2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)pent-4-ynoic acid
methyl 4-ethynylbenzoate
oct-7-ynoic acid
methyl 4-hydroxybut-2-ynoate
Total: 1775
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