Asymmetric synthesis of orobanchol, a representative canonical strigolactone, based on enzymatic kinetic resolution and its conversion to naturally occurring orobanchol derivatives.

MLA

Uchida, Kiyono, et al. “Asymmetric Synthesis of Orobanchol, a Representative Canonical Strigolactone, Based on Enzymatic Kinetic Resolution and Its Conversion to Naturally Occurring Orobanchol Derivatives.” Tetrahedron, vol. 159, June 2024, p. N.PAG. EBSCOhost, https://doi.org/10.1016/j.tet.2024.134016.

APA

Uchida, K., Okamura, H., Ogura, Y., & Takikawa, H. (2024). Asymmetric synthesis of orobanchol, a representative canonical strigolactone, based on enzymatic kinetic resolution and its conversion to naturally occurring orobanchol derivatives. Tetrahedron, 159, N.PAG. https://doi.org/10.1016/j.tet.2024.134016

Chicago

Uchida, Kiyono, Hironori Okamura, Yusuke Ogura, and Hirosato Takikawa. 2024. “Asymmetric Synthesis of Orobanchol, a Representative Canonical Strigolactone, Based on Enzymatic Kinetic Resolution and Its Conversion to Naturally Occurring Orobanchol Derivatives.” Tetrahedron 159 (June): N.PAG. doi:10.1016/j.tet.2024.134016.