Supporting Information
| Supporting Information File 1: Experimental section and time–conversion plots for formose reactions in the presence of SPB and pVPB/NaSS. | ||
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Cite the Following Article
Formose reaction controlled by boronic acid compounds
Toru Imai, Tomohiro Michitaka and Akihito Hashidzume
Beilstein J. Org. Chem. 2016, 12, 2668–2672.
https://doi.org/10.3762/bjoc.12.263
How to Cite
Imai, T.; Michitaka, T.; Hashidzume, A. Beilstein J. Org. Chem. 2016, 12, 2668–2672. doi:10.3762/bjoc.12.263
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Scholarly Works
- Hashidzume, A.; Imai, T.; Deguchi, N.; Tanibayashi, T.; Ikeda, T.; Michitaka, T.; Kuwahara, S.; Nakahata, M.; Kamon, Y.; Todokoro, Y. Preferential formation of specific hexose and heptose in the formose reaction under microwave irradiation. RSC advances 2023, 13, 4089–4095. doi:10.1039/d2ra07249a
- Barge, L. M.; Rodriguez, L. E.; Weber, J. M.; Theiling, B. P. Determining the "Biosignature Threshold" for Life Detection on Biotic, Abiotic, or Prebiotic Worlds. Astrobiology 2021, 22, 481–493. doi:10.1089/ast.2021.0079
- Michitaka, T.; Imai, T.; Hashidzume, A. Formose Reaction Controlled by a Copolymer of N,N-Dimethylacrylamide and 4-Vinylphenylboronic Acid. Polymers 2017, 9, 549.
- Michitaka, T.; Imai, T.; Hashidzume, A. Formose Reaction Controlled by a Copolymer of N,N-Dimethylacrylamide and 4-Vinylphenylboronic Acid. Polymers 2017, 9, 549. doi:10.3390/polym9110549
- Mlostoń, G.; Grzelak, P.; Linden, A.; Heimgartner, H. Thia-Diels–Alder reactions of hetaryl thioketones with nonactivated 1,3-dienes leading to 3,6-dihydro-2H-pyrans: evidence for a diradical mechanism. Chemistry of Heterocyclic Compounds 2017, 53, 518–525. doi:10.1007/s10593-017-2086-9
