Jiang, X. et al.: 2021 Science of Synthesis: Knowledge Updates 2020/3 DOI: 10.1055/sos-SD-114-00484
Knowledge Updates 2020/3

14.4.16 1H-2-Benzopyran-1-ones (Update 2020)

More Information

Book

Editors: Jiang, X.; Marschner, C.; Oestreich, M.; Wang, M.

Authors: An, K.; Arisetti, N.; Cheng, B.; Gao, W.-C.; He, W.; Jiang, B.; Krause, N.; Lu, J.; Marschner, C.; Shao, L.; Shi, T.; Tan, Q.; Tian, J.; Wang, T.; Wang, Z.; Wei, W.; Weinert, C.; Zhang, H.-H.; Zhang, Q.; Zhao, X.; Zhu, C.-F.

Title: Knowledge Updates 2020/3

Print ISBN: 9783132435643; Online ISBN: 9783132435667; Book DOI: 10.1055/b000000104

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Knowledge Updates



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G.; Nevado, C.; Trost, B. M.; You, S.

Type: Multivolume Edition

 

Abstract

This chapter is an update to the earlier Science of Synthesis contribution (Section 14.4.5) describing methods for the preparation of 1H-2-benzopyran-1-ones (isocoumarins) and their derivatives. The methods covered come from the literature published in the period 2003–2019.

 
  • 1 Saeed A., Mahesar P. A.. Tetrahedron 2014; 70: 1401
  • 2 Yuan Q., Chen Z.-B., Zhang F.-L., Zhu Y.-M.. Org. Biomol. Chem 2017; 15: 1628
  • 3 Fei X.-D., Ge Z.-Y., Tang T., Zhu Y.-M., Ji S.-J.. J. Org. Chem 2012; 77: 10 321
  • 4 Nakamura Y., Ukita T.. Org. Lett 2002; 4: 2317
  • 5 Ueura K., Satoh T., Miura M.. Org. Lett 2007; 9: 1407
  • 6 Mo J., Wang L., Cui X.. Org. Lett 2015; 17: 4960
  • 7 Li X. G., Liu K., Zou G., Liu P. N.. Adv. Synth. Catal 2014; 356: 1496
  • 8 Zhang S.-L., Yu Z.-L.. Org. Biomol. Chem 2016; 14: 10 511
  • 9 Liu L., Hu J., Wang X.-C., Zhong M.-J., Liu X.-Y., Yang S.-D., Liang Y.-M.. Tetrahedron 2012; 68: 5391
  • 10 Casnati A., Maggi R., Maestri G., Ca’ N. D., Motti E.. J. Org. Chem 2017; 82: 8296
  • 11 Li X. G., Sun M., Liu K., Jin Q., Liu P. N.. Chem. Commun. (Cambridge) 2015; 51: 2380
  • 12 Yu Y., Lu Q., Chen G., Li C., Huang X.. Angew. Chem. Int. Ed 2018; 57: 319
  • 13 Suzuki T., Yamada T., Watanabe K., Katoh T.. Bioorg. Med. Chem. Lett 2005; 15: 2583
  • 14 Kumar Y. S., Dasaradhan C., Prabakaran K., Manivel P., Khan F.-R. N., Jeong E. D., Chung E. H.. Tetrahedron Lett 2015; 56: 941
  • 15 Bihel F., Quéléver G., Lelouard H., Petit A., da Costa C. A., Pourquié O., Checler F., Thellend A., Pierre P., Kraus J.-L.. Bioorg. Med. Chem 2003; 11: 3141
  • 16 Panda N., Mishra P., Mattan I.. J. Org. Chem 2016; 81: 1047
  • 17 Alper P. B., Nguyen K. T.. J. Org. Chem 2003; 68: 2051
  • 18 Zhao J., Xu W., Xie X., Sun N., Li X., Liu Y.. Org. Lett 2018; 20: 5461