Relevant bibliographies by topics / Dibenzocyclooctyne

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  1. Journal articles

Academic literature on the topic 'Dibenzocyclooctyne'

Author: Grafiati
Published: 21 December 2024

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Journal articles on the topic "Dibenzocyclooctyne"

1

He, Yinming, Li Liu, and Liang Cheng. "A Short Review of Research Progress on the Synthesis Approaches of Aza-Dibenzocyclooctyne Derivatives." Molecules 28, no. 9 (2023): 3715. http://dx.doi.org/10.3390/molecules28093715.

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Cyclooctyne molecules have found wide applications in the strain-promoted azide–alkyne cycloaddition (SPAAC) reactions, which avoid the biotoxicity caused by the use of Cu(I) catalysts. Among the various cyclooctyne systems, dibenzocyclooctyne (DBCO) series have displayed the highest reaction activity. However, the synthesis processes of such structures are time-consuming, which to some extent limit their large-scale development and application. This review has summarized current synthesis routes of two DBCO molecules, aza-dibenzocyclooctyne (DIBAC) and biarylazacyclooctynone (BARAC).
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2

Narayanam, Maruthi Kumar, Yong Liang, K. N. Houk, and Jennifer M. Murphy. "Discovery of new mutually orthogonal bioorthogonal cycloaddition pairs through computational screening." Chemical Science 7, no. 2 (2016): 1257–61. http://dx.doi.org/10.1039/c5sc03259h.

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3

Shenje, Learnmore, Yingqi Qu, Vladimir Popik, and Susanne Ullrich. "Femtosecond photodecarbonylation of photo-ODIBO studied by stimulated Raman spectroscopy and density functional theory." Physical Chemistry Chemical Physics 23, no. 45 (2021): 25637–48. http://dx.doi.org/10.1039/d1cp03512f.

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4

Adronov, Alex, Kelvin Li, and Stuart McNelles. "Preparation and Properties of a Hydrolytically Stable Cyclooctyne-Containing Polymer." Synlett 29, no. 19 (2018): 2535–41. http://dx.doi.org/10.1055/s-0037-1610636.

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A poly[(phenylene vinylene)-co-dibenzocyclooctyne] polymer prepared by Wittig polymerization chemistry between dibenzocyclooctyne bisaldehyde [DIBO-(CHO)2] and bis(triethyleneglycol)phenylbis(tributylphosphonium) dibromide is reported. The resulting polymer exhibits moderate molecular weight (Mn: 10.5 kDa, Mw: 21.3 kDa, Ð: 2.02) and is fluorescent. It could be readily functionalized by strain-promoted alkyne-azide cycloadditon with different azides, and fluorescence of the polymer was preserved after functionalization. Grafting azide-terminated 5 kDa poly(ethylene glycol) monomethyl ether chai
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5

Wang, Mengzhe, Christopher D. McNitt, Hui Wang, et al. "The efficiency of 18F labelling of a prostate specific membrane antigen ligand via strain-promoted azide–alkyne reaction: reaction speed versus hydrophilicity." Chemical Communications 54, no. 56 (2018): 7810–13. http://dx.doi.org/10.1039/c8cc03999b.

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6

Kardelis, Vladimir, Ryan C. Chadwick, and Alex Adronov. "Click Functionalization of a Dibenzocyclooctyne-Containing Conjugated Polyimine." Angewandte Chemie International Edition 55, no. 3 (2015): 945–49. http://dx.doi.org/10.1002/anie.201508639.

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7

Kardelis, Vladimir, Ryan C. Chadwick, and Alex Adronov. "Click Functionalization of a Dibenzocyclooctyne-Containing Conjugated Polyimine." Angewandte Chemie 128, no. 3 (2015): 957–61. http://dx.doi.org/10.1002/ange.201508639.

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8

Moran, Joseph, Craig S. McKay, and John Paul Pezacki. "Strain-promoted 1,3-dipolar cycloadditions of diazo compounds with cyclooctynes." Canadian Journal of Chemistry 89, no. 2 (2011): 148–51. http://dx.doi.org/10.1139/v10-112.

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Strain-promoted cycloadditions of diazo compounds with dibenzocyclooctyne proceed with second-order rate constants of >10 L mol–1 s–1 at 25 °C. These reactions display rate constants that are comparable or greater than those of the analogous reactions of nitrones or azides with cyclooctynes.
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9

Kettenbach, K., and T. L. Ross. "A 18F-labeled dibenzocyclooctyne (DBCO) derivative for copper-free click labeling of biomolecules." MedChemComm 7, no. 4 (2016): 654–57. http://dx.doi.org/10.1039/c5md00508f.

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The new prosthetic group <sup>18</sup>F-TEG-DBCO (dibenzocyclooctyne) can be prepared within a total reaction time of 60 min including purification with an overall yield (n.d.c.) of 34 ± 5%. Copper-free click cycloadditions with various biomolecule-azides resulted in very high RCYs under mild conditions.
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10

Djurdjevic, Sinisa, and James R. Green. "Nicholas Reactions in the Synthesis of Dicobalt Dibenzocyclooctyne Complexes." Organic Letters 15, no. 21 (2013): 5468–71. http://dx.doi.org/10.1021/ol402617a.

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