The aerobic oxidation reactions of alcohols 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 15th 2023.
Hua Fu et al. RSC Adv. 2012, 2, 6549–6554; RSC Advances 2012, 2, 11061–11066.
Gerhard Hilt et al. Org. Lett. 2017, 19, 564−567.
Bo Liu et al. Chem. Commun. 2017, 53, 5549−5552.
Frank Glorius et al. ACS Catal. 2018, 8, 10036−10042.
Elisabetta Brenna et al. Adv. Synth. Catal. 2019, 361, 2638–2648.
Jian-Hua Xie et al. Org. Lett. 2022, 24, 5161−5165.
M. Kevin Brown et al. J. Am. Chem. Soc. 2022, 144, 18790–18796.
B. A. Trofimov et al. Chem. Heterocycl. Compd. 2013, 49, 341–344.
Xiao-Song Xue & Peng Wang et al. Angew. Chem. Int. Ed. 2023, 62, e202216373.
Shufeng Chen et al. Org. Biomol. Chem. 2019, 17, 789-793.
Manolis Stratakis et al. Org. Lett. 2019, 21, 5552−5555.
Shi-Kai Tian et al. J. Org. Chem. 2021, 86, 3065−3073.
Jia-Hua chen & Zhen Yang et al. J. Org. Chem. 2018, 83, 6893−6906.
Rai-Shung Liu et al. Org. Lett. 2018, 20, 1038−1041. (Formal synthesis of fluvastatin)
Pu-Sheng Wang et al. Chem. Lett. 2017, 46, 1190−1192. (Formal synthesis of gonytolide C)
Bernd Plietker et al. Org. Lett. 2018, 20, 4328−4331.
Jian Liao et al. Org. Lett. 2018, 20, 1346−1349. (Synthesis of Naproxen and formal synthesis of 8-deoxyanisatin)
Jiaxin Zhang & Peng Jiao et al. Beilstein J. Org. Chem. 2019, 15, 1840–1847.
Changwu Zheng & Gang Zhao et al. Angew. Chem. Int. Ed. 2021, 60, 23641–23645.
Katalin Barta & Ben L. Feringa et al. Green Chem. 2022, 24, 3689–3696. (Synthesis of molecular motor)
Héctor D. Abruña, Scott L. Anderson & Phil S. Baran et al. Science 2022, 375, 745–752.