The ATA reaction developed by this group has been used by over 100 groups in their research projects. The details are shown as follows:

The data shown bellow were collected on March 15^th 2023.

Syntheses of mono-substituted allenes

Carsten Bolm et al. Faraday Discuss. 2023, 241, 79; Green Chem. 2022, 24, 3125.

Yao Fu & Yun-He Xu et al. J. Am. Chem. Soc. 2022, 144, 5535.

Martín Fañanás-Mastral et al. J. Am. Chem. Soc. 2022, 144, 16206.

Biao Yu et al. Tetrahedron 2022, 129, 133145.

Poonsakdi Ploypradith et al. J. Org. Chem. 2022, 87, 15863.

Zong-Quan Wu & Gao-Wei Li et al. Polymer 2022, 245, 124712

Zong-Quan Wu & Li Zhou et al. Polym. Chem. 2021, 12, 4822.

K. C. Kumara Swamy et al. J. Org. Chem. 2022, 87, 13683; Synthesis 2014, 46, 1091.

Zhuang-Ping Zhan et al. J. Org. Chem. 2022, 87, 1589; Org. Lett. 2022, 24, 1195.

Moisés Gulías & José Luis Mascareñas et al. J. Am. Chem. Soc. 2022, 144, 21437.

Changkun Li et al. Org. Chem. Front. 2022, 9, 6869.

Zhong-Xia Wang et al. Org. Lett. 2022, 24, 7934; Org. Lett. 2022, 24, 692; Adv. Synth. Catal. 2022, 364, 2753.

Chandra M. R. Volla et al. Org. Lett. 2022, 24, 8936; Angew. Chem. Int. Ed. 2020, 59, 17042.

Santanu Mukherjee et al. Angew. Chem. Int. Ed. 2022, 61, e202115821.

Pengxiang Xu & Yuxing Gao & Yufen Zhao et al. Chem. Commun. 2021, 57, 339.

Chuanming Yu et al. Org. Biomol. Chem. 2021, 19, 7701.

Yi-Ming Wang et al. J. Am. Chem. Soc. 2021, 143, 14998.

Thomas Magauer et al. Chem.Eur. J. 2021, 27, 12410.

Shaozhong Ge et al. Angew. Chem. Int. Ed. 2021, 60, 2149.

Zhaomin Hou et al.ACS Catal. 2020, 10, 11685.

Amir H. Hoveyda et al. J. Am. Chem. Soc. 2020, 142, 18200.

Vladimir A. D’yakonov et al. J. Nat. Prod. 2020, 83, 2399.

Urs Gellrich et al. Angew. Chem. Int. Ed. 2020, 59, 23885.

Darren J. Dixon et al. Chem. Sci. 2020, 11, 7444.

Amir H. Hoveyda et al. J. Am. Chem. Soc. 2020, 142, 436.

Gerhard Erker et al. Chem. Sci. 2020, 11, 1542.

Rene M. Koenigs et al. Org. Lett. 2020, 22, 4873.

Manolis Stratakis et al. Org. Lett. 2019, 21, 5552.

Bernhard Breit et al. Angew. Chem. Int. Ed. 2019, 58, 9994.

Toshimasa Itoh et al. Bioorganic & Medicinal Chemistry 2019, 27, 285.

Giuseppe Zanoni & Debabrata Maiti et al. Chem. Eur. J. 2019, 25, 750.

Gerald B. Hammond & Bo Xu et al. Green Chem. 2019, 21, 1467.

Vincent Gandon & Emmanuel Roulland et al. Org. Lett. 2019, 21, 3141.

Robert R. Knowles et al. J. Am. Chem. Soc. 2019, 141, 8752.

Gerhard Erker et al. Chem. Commun. 2019, 55, 10166.

Gerhard Erker et al. Angew. Chem. Int. Ed. 2018, 57, 13922

Yan He et al. J. Org. Chem. 2018, 83, 12514

Lilya U. Dzhemileva & Vladimir A. D’yakonov et al. Org. Biomol. Chem. 2017, 15, 470.

Vladimir A. D’yakonov et al. Mendeleev Commun. 2017, 27, 122.

Vladimir A. D’yakonov et al. Tetrahedron Lett. 2017, 58, 1755.

Dirk Trauner et al. J. Am. Chem. Soc. 2017, 139, 4117.

Tsuyoshi Mita & Yoshihiro Sato et al. Org. Lett. 2017, 19, 2170.

Takashi Koike & Munetaka Akita et al. Chem. Commun. 2017, 53, 4681.

Emmanuel Roulland et al. Org. Lett. 2017, 19, 4006.

Anna Pla-Quintana et al. Chem. Commun. 2017, 53, 9922.

MiquelSol, AnnaPla-Quintana, and AnnaRoglans et al. Chem. Eur. J. 2017, 23, 14889.

Gojko Lalic et al. Angew. Chem. Int. Ed. 2017, 56, 15703.

Rai-Shung Liu et al. Org. Biomol. Chem. 2017, 15, 9389.

Mingji Dai Tetrahedron 2017, 73, 4172

Vladimir A. D’yakonov et al. Tetrahedron 2016, 72, 5783.

Vladimir A. D’yakonov et al. J. Nat. Prod. 2016, 79, 2039.

Zhi-Xiang Yu et al. Org. Biomol. Chem. 2016, 14, 5945.

Peng R. Chen et al. J. Am. Chem. Soc. 2016, 138, 15118.

Jin Zhu et al. Org. Lett. 2016, 18, 3806.

Stephen L. Buchwald et al. Angew. Chem. Int. Ed. 2016, 55, 14077

Henk Hiemstra et al. Chem. Eur. J. 2016, 22, 1266

Kuiling Ding et al. J. Am. Chem. Soc. 2015, 137, 15346.

Erik J. Alexanian et al. Org. Lett. 2015, 17, 1284.

Bernhard Breit et al. Angew. Chem. Int. Ed. 2015, 54, 7149.

Anna Roglans & Anna Pla-Quintana et al. Org. Lett. 2015, 17, 2882.

Christopher J. Cordier et al. Angew. Chem. Int. Ed. 2015, 54, 13734.

Xinying Zhang & Xuesen Fan et al. Chem. Commun. 2015, 51, 16263

Ullrich Jahn et al. Angew. Chem. Int. Ed. 2015, 54, 12153

Paul R. Raithby & Chick C. Wilson et al. CrystEngComm 2015, 17, 8139

Henk Hiemstra et al. Org. Lett. 2015, 17, 3892

Zhaomin Hou et al. Chem. Eur. J. 2015, 21, 8394

Xavier Guinchard et al. Chem. Eur. J. 2015, 21, 8511

Min Shi et al. Org. Chem. Front. 2015, 2, 394

Bernhard Breit et al. Angew. Chem. Int. Ed. 2014, 53, 13780.

Yasushi Tsuji et al. Angew. Chem. Int. Ed. 2014, 53, 9007.

Seiji Iwasa et al. Org. Lett. 2014, 16, 3408.

Ronald Grigg et al. Tetrahedron 2014, 70, 4394.

Kumara Swamy et al. Synthesis 2014, 46, 1091

Miquel Solà & Anna Pla-Quintana et al. Chem. Eur. J. 2014, 20, 5034

Ronald Grigg Tetrahedron 2014, 70, 4934

Ronald Grigg Tetrahedron 2014, 70, 110

Tuomo Leikoski et al. Can. J. Chem. 2013, 91, 38.

Zhongwen Wang et al. Org. Lett. 2013, 15, 5682.

Yasushi Tsuji et al. Angew. Chem. Int. Ed. 2013, 52, 12400.

A. Stephen K. Hashmi et al. Adv. Synth. Catal. 2013, 355, 1383

Xavier Ariza & Jordi Garcia et al. J. Org. Chem. 2013, 78, 1519

Gu Yuan et al. Can. J. Chem. 2012, 90, 38

Ronald Grigg et al. Chem. Commun. 2012, 48, 11504

Patrick J. Guiry et al. J. Org. Chem. 2011, 76, 3536

Xavier Ariza & Jordi Garcia Tetrahedron 2011, 67, 5184

Hideki Yorimitsu & Koichiro Oshima et al. J. Am. Chem. Soc. 2010, 132, 8878

William R. Roush et al. J. Am. Chem. Soc. 2009, 131, 14174

Zong-Quan Wu et al. Macromolecules 2021, 54, 679.

Chandra M. R. Volla et al. Angew. Chem. Int. Ed. 2020, 59, 17042.

VisuvanatharSridharan et al. Tetrahedron Lett. 2020, 61, 152536.

Giovanni Maestri et al. Org. Lett. 2020, 22, 6354.

Lunjian Chen & Hongbin Zhai et al. Chem. Commun. 2020, 56, 3405.

Chunji Wu, Laurent Maron, and Dongmei Cui et al. Angew. Chem. Int. Ed. 2020, 59, 4947.

Robert J. McMahon et al. J. Org. Chem. 2020, 85, 5787.

Peter Wipf et al. Org. Lett. 2020, 22, 2215.

Shigeru Arai et al. Adv. Synth. Catal. 2019, 361, 4882.

Erick M. Carreira et al. J. Am. Chem. Soc. 2019, 141, 4738

Erick M. Carreira et al. J. Am. Chem. Soc. 2018, 140, 4697

D. Listunov, Yves Génisson, Valérie Maraval, Remi Chauvin et al. ChemMedChem 2018, 13, 1711

Giuseppe Zanoni & Liming Zhang et al. J. Am. Chem. Soc. 2017, 139, 16064.

Bruce H. Lipshutz et al. Angew. Chem. Int. Ed. 2017, 56, 847.

Rai-Shung Liu et al. Org. Lett. 2017, 19, 5340.

Yu Rao et al. Org. Lett. 2017, 19, 972.

Michel R. Gagné et al. Org. Lett. 2017, 19, 6256.

Jan-E. Bäckvall et al. Angew. Chem. Int. Ed. 2016, 55, 5568.

Hai-Chao Xu et al. Eur. J. Org. Chem. 2016, 3449.

Youngmin You & Eun Joo Kang et al. Org. Lett. 2016, 18, 4900.

Ai-Lan Lee et al. J. Org. Chem. 2015, 80, 1703.

Zhaomin Hou et al. Chem. Eur. J. 2015, 21, 8394.

Vladimir A. D’yakonov & Lilya U. Dzhemileva et al. Steroids 2015, 102, 110.

Vladimir A. D’yakonov et al. Russian Chemical Bulletin 2015, 64, 2135.

Magnus W.P. Bebbington et al. Tetrahedron 2015, 71, 727.

Xavier Guinchard et al. Chem. Eur. J. 2015, 21, 8511.

Rai-Shung Liu et al. Chem. Eur. J. 2015, 21, 4590

Martin G. Banwell et al. Chem. Asian J. 2014, 9, 67.

David J. Procter et al. Chem. Eur. J. 2014, 20, 13143.

Xavier Ariza & Jordi Garcia et al. J. Org. Chem. 2014, 79, 9578

Timothy F. Jamison et al. Tetrahedron 2013, 69, 5205.

Jianbo Wang et al. Angew. Chem. Int. Ed. 2013, 52, 9305.

Elvira E. Shults et al. ChemistryOpen 2018, 7, 890.

Hironao Sajiki & Yoshinari Sawama et al. ChemistrySelect 2017, 2, 876.

Xinying Zhang & Xuesen Fan et al. Chem. Commun. 2015, 51, 16263

Eric Clot & Lutz H. Gade et al. Chem. Eur. J. 2015, 21, 18730.

---

Syntheses of racemic 1,3-disubstituted allenes

Shi-Kai Tian et al. Org. Biomol. Chem. 2021, 19, 5353; Chem. Commun. 2012, 48, 10913

Giovanni Maestri et al. Org. Lett. 2020, 22, 6354.

Congrong Liu et al. Chin. J. Chem. 2018, 36, 737.

Mingji Dai et al. Angew. Chem. Int. Ed. 2017, 56, 11624.

Graham K. Murphy et al. Angew. Chem. Int. Ed. 2017, 56, 11620.

MiquelSol, AnnaPla-Quintana, and AnnaRoglans et al. Chem. Eur. J. 2017, 23, 14889.

Klaus T. Wanner et al. J. Org. Chem. 2017, 82, 8371.

Manolis Stratakis et al. Org. Lett. 2015, 17, 4538.

Hanmin Huang et al. Angew. Chem. Int. Ed. 2014, 53, 7272.

Xavier Guinchard et al. Org. Lett. 2014, 16, 5438.

Marıa Paz Munoz et al. Chem. Commun. 2014, 50, 1494.

Shufeng Chen & Baoguo Li Appl. Organometal. Chem. 2012, 26, 284.

María Paz Muñoz et al. Chem. Eur. J. 2012, 18, 4499.

Bo Xu & Gerald B. Hammond et al. J. Org. Chem. 2012, 77, 7725.

Shi-Kai Tian et al. Chem. Commun. 2012, 48, 10913.

José L. Mascareñas et al. Angew. Chem. Int. Ed. 2011, 50, 11496.

José L. Mascareñas et al. J. Am. Chem. Soc. 2011, 133, 7660.

María Paz Muñoz et al. Adv. Synth. Catal. 2010, 352, 2189.

Xinying Zhang & Xuesen Fan et al. Chem. Commun. 2015, 51, 16263.

---

Syntheses of racemic trisubstituted allenes

Jan-E. Bäckvall et al. Angew. Chem. Int. Ed. 2015, 54, 9066.

Ben L. Feringa et al. Angew. Chem. Int. Ed. 2020, 59, 7823.

Georgios C. Vougioukalakis et al. ACS Omega 2019, 4, 10279.

Klaus T. Wanner et al. ChemMedChem 2019, 14, 1135.

---

Syntheses of chiral 1,3-disubstituted allenes

Shigeru Arai et al. Org. Biomol. Chem. 2017, 15, 1612.

Rai-Shung Liu et al. Org. Biomol. Chem. 2017, 15, 9389.

Kamal Kumar & Herbert Waldmann et al. Angew. Chem. Int. Ed. 2014, 53, 8122.

Stéphanie Ballereau et al. Synlett 2019, 30, 185.

D. Listunov, Yves Génisson, Valérie Maraval, Remi Chauvin et al. ChemMedChem 2018, 13, 1711.

Ai-Lan Lee et al. Chem. Eur. J. 2016, 22, 18593.