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The University of San Francisco

Chemistry Faculty Publications

2017

Articles 1 - 2 of 2

Full-Text Articles in Chemistry

A Redox-Neutral Catechol Synthesis, Q. Wu, D. Yan, Y. Chen, T. Wang, F. Xiong, W. Wei, Y. Lu, W. Sun, Jie Jack Li, J. Zhao Jan 2017

A Redox-Neutral Catechol Synthesis, Q. Wu, D. Yan, Y. Chen, T. Wang, F. Xiong, W. Wei, Y. Lu, W. Sun, Jie Jack Li, J. Zhao

Chemistry Faculty Publications

Ubiquitous tyrosinase catalyses the aerobic oxidation of phenols to catechols through the binuclear copper centres. Here, inspired by the Fischer indole synthesis, we report an iridium-catalysed tyrosinase-like approach to catechols, employing an oxyacetamide-directed C–H hydroxylation on phenols. This method achieves one-step, redox-neutral synthesis of catechols with diverse substituent groups under mild conditions. Mechanistic studies confirm that the directing group (DG) oxyacetamide acts as the oxygen source. This strategy has been applied to the synthesis of different important catechols with fluorescent property and bioactivity from the corresponding phenols. Finally, our method also provides a convenient route to 18O-labelled catechols using …


A Bioinspired And Biocompatible Ortho-Sulfiliminyl Phenol Synthesis, Feng Xiong, Liang Lu, Tian-Yu Sun, Qian Wu, Dingyuan Yan, Ying Chen, Xinhao Zhang, Wei Wei, Yi Lu, Wei-Yin Sun, Jie Jack Li, Jing Zhao Jan 2017

A Bioinspired And Biocompatible Ortho-Sulfiliminyl Phenol Synthesis, Feng Xiong, Liang Lu, Tian-Yu Sun, Qian Wu, Dingyuan Yan, Ying Chen, Xinhao Zhang, Wei Wei, Yi Lu, Wei-Yin Sun, Jie Jack Li, Jing Zhao

Chemistry Faculty Publications

Synthetic methods inspired by Nature often offer unique advantages including mild conditions and biocompatibility with aqueous media. Inspired by an ergothioneine biosynthesis protein EgtB, a mononuclear non-haem iron enzyme capable of catalysing the C–S bond formation and sulfoxidation, herein, we discovered a mild and metal-free C–H sulfenylation/intramolecular rearrangement cascade reaction employing an internally oxidizing O–N bond as a directing group. Our strategy accommodates a variety of oxyamines with good site selectivity and intrinsic oxidative properties. Combining an O–N bond with an X–S bond generates a C–S bond and an S¼N bond rapidly. The newly discovered cascade reaction showed excellent chemoselectivity …