Stereoselective construction of tetra-substituted tetrahydrofuran compounds from benzylic hemiacetal in the presence of H2 and a Pd catalyst: stereoselective synthesis of a stereoisomer of (-)-virgatusin and its antimicrobiological activity.

MLA

Nakato, Tomofumi, et al. “Stereoselective Construction of Tetra-Substituted Tetrahydrofuran Compounds from Benzylic Hemiacetal in the Presence of H2 and a Pd Catalyst: Stereoselective Synthesis of a Stereoisomer of (-)-Virgatusin and Its Antimicrobiological Activity.” Bioscience, Biotechnology, and Biochemistry, vol. 72, no. 1, Jan. 2008, pp. 197–203. EBSCOhost, https://doi.org/10.1271/bbb.70554.

APA

Nakato, T., Tago, R., Akiyama, K., Maruyama, M., Sugahara, T., Kishida, T., & Yamauchi, S. (2008). Stereoselective construction of tetra-substituted tetrahydrofuran compounds from benzylic hemiacetal in the presence of H2 and a Pd catalyst: stereoselective synthesis of a stereoisomer of (-)-virgatusin and its antimicrobiological activity. Bioscience, Biotechnology, and Biochemistry, 72(1), 197–203. https://doi.org/10.1271/bbb.70554

Chicago

Nakato, Tomofumi, Ryosuke Tago, Koichi Akiyama, Masafumi Maruyama, Takuya Sugahara, Taro Kishida, and Satoshi Yamauchi. 2008. “Stereoselective Construction of Tetra-Substituted Tetrahydrofuran Compounds from Benzylic Hemiacetal in the Presence of H2 and a Pd Catalyst: Stereoselective Synthesis of a Stereoisomer of (-)-Virgatusin and Its Antimicrobiological Activity.” Bioscience, Biotechnology, and Biochemistry 72 (1): 197–203. doi:10.1271/bbb.70554.