ChemInform Abstract: Asymmetric Nucleophilic Acylation with Metalated Amino Nitriles: Diastereo- and Enantioselective Synthesis of 2-Substituted 3- Aroylcyclohexanones via Tandem Michael Addition/α-Alkylation.

MLA

Enders, D., et al. “ChemInform Abstract: Asymmetric Nucleophilic Acylation with Metalated Amino Nitriles: Diastereo- and Enantioselective Synthesis of 2-Substituted 3- Aroylcyclohexanones via Tandem Michael Addition/α-Alkylation.” ChemInform, vol. 26, no. 45, Nov. 1995, p. no. EBSCOhost, https://doi.org/10.1002/chin.199545100.

APA

Enders, D., Kirchhoff, J., Mannes, D., & Raabe, G. (1995). ChemInform Abstract: Asymmetric Nucleophilic Acylation with Metalated Amino Nitriles: Diastereo- and Enantioselective Synthesis of 2-Substituted 3- Aroylcyclohexanones via Tandem Michael Addition/α-Alkylation. ChemInform, 26(45), no. https://doi.org/10.1002/chin.199545100

Chicago

Enders, D., J. Kirchhoff, D. Mannes, and G. Raabe. 1995. “ChemInform Abstract: Asymmetric Nucleophilic Acylation with Metalated Amino Nitriles: Diastereo- and Enantioselective Synthesis of 2-Substituted 3- Aroylcyclohexanones via Tandem Michael Addition/α-Alkylation.” ChemInform 26 (45): no. doi:10.1002/chin.199545100.