Retention of stereochemistry in the microwave assisted synthesis of 1H-tetrazole bioisosteric moiety from chiral phenyl-acetic acid derivatives.

MLA

Tomassetti, Mara, et al. “Retention of Stereochemistry in the Microwave Assisted Synthesis of 1H-Tetrazole Bioisosteric Moiety from Chiral Phenyl-Acetic Acid Derivatives.” Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry, vol. 54, no. 46, Nov. 2013, pp. 6247–50. EBSCOhost, https://doi.org/10.1016/j.tetlet.2013.09.022.

APA

Tomassetti, M., Fanì, M., Bianchini, G., Giuli, S., Aramini, A., Colagioia, S., Nano, G., & Lillini, S. (2013). Retention of stereochemistry in the microwave assisted synthesis of 1H-tetrazole bioisosteric moiety from chiral phenyl-acetic acid derivatives. Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry, 54(46), 6247–6250. https://doi.org/10.1016/j.tetlet.2013.09.022

Chicago

Tomassetti, Mara, Michela Fanì, Gianluca Bianchini, Sandra Giuli, Andrea Aramini, Sandro Colagioia, Giuseppe Nano, and Samuele Lillini. 2013. “Retention of Stereochemistry in the Microwave Assisted Synthesis of 1H-Tetrazole Bioisosteric Moiety from Chiral Phenyl-Acetic Acid Derivatives.” Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry 54 (46): 6247–50. doi:10.1016/j.tetlet.2013.09.022.