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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Transient Protection of Organic Azides from Click Reactions with Alkynes by Phosphazide Formation
Tomohiro Meguro, Suguru Yoshida, Kazunobu Igawa, et al.
Organic Letters (2018) Vol. 20, Iss. 13, pp. 4126-4130
Closed Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Mechanisms and Substituent Effects of Metal-Free Bioorthogonal Reactions
Titas Deb, Julian Tu, Raphael M. Franzini
Chemical Reviews (2021) Vol. 121, Iss. 12, pp. 6850-6914
Closed Access | Times Cited: 96
Site-selective conversion of azido groups at carbonyl α-positions into oxime groups leading triazide to a triple click conjugation scaffold
Taiki Yokoi, Tomomi Ueda, Hiroki Tanimoto, et al.
Chemical Communications (2018) Vol. 55, Iss. 13, pp. 1891-1894
Closed Access | Times Cited: 32
Sequential conjugation methods based on triazole formation and related reactions using azides
Suguru Yoshida
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 8, pp. 1550-1562
Open Access | Times Cited: 32
Surface Functionalization of Black Phosphorus with Nitrenes: Identification of P=N Bonds by Using Isotopic Labeling
Kendahl L. Walz Mitra, Christine Chang, Michael P. Hanrahan, et al.
Angewandte Chemie International Edition (2020) Vol. 60, Iss. 16, pp. 9127-9134
Open Access | Times Cited: 29
Site-Selective Conversion of Azido Groups at Carbonyl α-Positions to Diazo Groups in Diazido and Triazido Compounds
Taiki Yokoi, Hiroki Tanimoto, Tomomi Ueda, et al.
The Journal of Organic Chemistry (2018) Vol. 83, Iss. 19, pp. 12103-12121
Closed Access | Times Cited: 27
Reactions of α-haloacroleins with azides: highly regioselective synthesis of formyl triazoles
Dongsheng Zhang, Yingzhu Fan, Zhongliang Yan, et al.
Green Chemistry (2019) Vol. 21, Iss. 15, pp. 4211-4216
Closed Access | Times Cited: 24
An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine–Azide Bioconjugation Method
Hisham M. El‐Shaffey, Elizabeth J. Gross, Yvonne Hall, et al.
Journal of the American Chemical Society (2021) Vol. 143, Iss. 33, pp. 12974-12979
Closed Access | Times Cited: 20
Spot the difference in reactivity: a comprehensive review of site-selective multicomponent conjugation exploiting multi-azide compounds
Hiroki Tanimoto, Takenori Tomohiro
Chemical Communications (2024)
Open Access | Times Cited: 2
Further enhancement of the clickability of doubly sterically-hindered aryl azides by para-amino substitution
Suguru Yoshida, Junko Tanaka, Yoshitake Nishiyama, et al.
Chemical Communications (2018) Vol. 54, Iss. 96, pp. 13499-13502
Open Access | Times Cited: 23
Effect of Resonance on the Clickability of Alkenyl Azides in the Strain-promoted Cycloaddition with Dibenzo-fused Cyclooctynes
Suguru Yoshida, Sayuri Goto, Yoshitake Nishiyama, et al.
Chemistry Letters (2019) Vol. 48, Iss. 9, pp. 1038-1041
Open Access | Times Cited: 20
A facile preparation of functional cycloalkynes via an azide-to-cycloalkyne switching approach
Suguru Yoshida, Tomoko Kuribara, Harumi Ito, et al.
Chemical Communications (2019) Vol. 55, Iss. 24, pp. 3556-3559
Open Access | Times Cited: 19
Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations
Suguru Yoshida, Yuki Sakata, Yoshihiro Misawa, et al.
Chemical Communications (2020) Vol. 57, Iss. 7, pp. 899-902
Closed Access | Times Cited: 16
Modular activatable bioorthogonal reagents
Pratik Kumar, Scott T. Laughlin
Methods in enzymology on CD-ROM/Methods in enzymology (2019), pp. 153-182
Closed Access | Times Cited: 16
Facile assembly of three cycloalkyne-modules onto a platform compound bearing thiophene S,S-dioxide moiety and two azido groups
Tomohiro Meguro, Yuki Sakata, Takamoto Morita, et al.
Chemical Communications (2020) Vol. 56, Iss. 34, pp. 4720-4723
Open Access | Times Cited: 15
Taming the reactivity of alkyl azides by intramolecular hydrogen bonding: site-selective conjugation of unhindered diazides
Koshiro Maegawa, Hiroki Tanimoto, Seiji Onishi, et al.
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 20, pp. 5793-5803
Open Access | Times Cited: 13
Site-specific DNA functionalization through the tetrazene-forming reaction in ionic liquids
Seiya Ishizawa, Munkhtuya Tumurkhuu, Elizabeth J. Gross, et al.
Chemical Science (2022) Vol. 13, Iss. 6, pp. 1780-1788
Open Access | Times Cited: 9
Chemodivergent Staudinger Reactions of Secondary Phosphine Oxides and Application to the Total Synthesis of LL–D05139β Potassium Salt
Wenjun Luo, Fang Xu, Zhenguo Wang, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 41
Closed Access | Times Cited: 5
Triazole formation of phosphinyl alkynes with azides through transient protection of phosphine by copper
Norikazu Terashima, Yuki Sakata, Tomohiro Meguro, et al.
Chemical Communications (2020) Vol. 56, Iss. 90, pp. 14003-14006
Closed Access | Times Cited: 14
Conversion of Alkyl Azides to Diazo Compounds and the Azide-Site Selectivity: One-Pot Phosphine-Mediated Transient Protection of Azido Groups and Deprotective Transformation to Diazo Groups
Hiroki Tanimoto, R. Adachi, Kodai Tanisawa, et al.
(2024)
Open Access | Times Cited: 1
Amphos-Mediated Conversion of Alkyl Azides to Diazo Compounds and One-Pot Azide-Site Selective Transient Protection, Click Conjugation, and Deprotective Transformation
Hiroki Tanimoto, R. Adachi, Kodai Tanisawa, et al.
Organic Letters (2024) Vol. 26, Iss. 12, pp. 2409-2413
Open Access | Times Cited: 1
Selective strain-promoted azide–alkyne cycloadditions through transient protection of bicyclo[6.1.0]nonynes with silver or gold
Keisuke Adachi, Tomohiro Meguro, Yuki Sakata, et al.
Chemical Communications (2020) Vol. 56, Iss. 68, pp. 9823-9826
Open Access | Times Cited: 10
2-Azidoacrylamides as compact platforms for efficient modular synthesis
Hinano Takemura, Sayuri Goto, Takamitsu Hosoya, et al.
Chemical Communications (2020) Vol. 56, Iss. 99, pp. 15541-15544
Closed Access | Times Cited: 10
Nucleophilic transformations of azido-containing carbonyl compounds via protection of the azido group
Takahiro Aimi, Tomohiro Meguro, Akihiro Kobayashi, et al.
Chemical Communications (2021) Vol. 57, Iss. 49, pp. 6062-6065
Open Access | Times Cited: 8
Continuous Flow Synthesis of Non‐Symmetrical Ureas from CO2
Alexandre Labiche, Maylis Norlöff, Sophie Feuillastre, et al.
Asian Journal of Organic Chemistry (2023) Vol. 12, Iss. 3
Open Access | Times Cited: 3
Synthesis of 1,2,3-triazoles using Grignard reactions through the protection of azides
Rina Namioka, Minori Suzuki, Suguru Yoshida
Frontiers in Chemistry (2023) Vol. 11
Open Access | Times Cited: 3
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