Efficient synthesis of 5,6-dihydroxyindole dimers, key eumelanin building blocks, by a unified o-ethynylaniline-based strategy for the construction of 2-linked biindolyl scaffolds.

MLA

Capelli, Luigia, et al. “Efficient Synthesis of 5,6-Dihydroxyindole Dimers, Key Eumelanin Building Blocks, by a Unified o-Ethynylaniline-Based Strategy for the Construction of 2-Linked Biindolyl Scaffolds.” The Journal of Organic Chemistry, vol. 74, no. 18, Sept. 2009, pp. 7191–94. EBSCOhost, https://doi.org/10.1021/jo901259s.

APA

Capelli, L., Manini, P., Pezzella, A., Napolitano, A., & d’Ischia, M. (2009). Efficient synthesis of 5,6-dihydroxyindole dimers, key eumelanin building blocks, by a unified o-ethynylaniline-based strategy for the construction of 2-linked biindolyl scaffolds. The Journal of Organic Chemistry, 74(18), 7191–7194. https://doi.org/10.1021/jo901259s

Chicago

Capelli, Luigia, Paola Manini, Alessandro Pezzella, Alessandra Napolitano, and Marco d’Ischia. 2009. “Efficient Synthesis of 5,6-Dihydroxyindole Dimers, Key Eumelanin Building Blocks, by a Unified o-Ethynylaniline-Based Strategy for the Construction of 2-Linked Biindolyl Scaffolds.” The Journal of Organic Chemistry 74 (18): 7191–94. doi:10.1021/jo901259s.