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Academic literature on the topic 'Leuckart Reaction'
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Journal articles on the topic "Leuckart Reaction"
Umar, Qasim, and Mei Luo. "A Brief Review: Advancement in the Synthesis of Amine through the Leuckart Reaction." Reactions 4, no. 1 (2023): 117–47. http://dx.doi.org/10.3390/reactions4010007.
Full textBokale-Shivale, Suvarna, Mohammad A. Amin, Rajiv T. Sawant, et al. "Synthesis of substituted 3,4-dihydroquinazolinones via a metal free Leuckart–Wallach type reaction." RSC Advances 11, no. 1 (2021): 349–53. http://dx.doi.org/10.1039/d0ra10142g.
Full textLejon, Tore, Irene Helland, Wang Liufang, et al. "Effect of Formamide in the Leuckart Reaction." Acta Chemica Scandinavica 53 (1999): 76–78. http://dx.doi.org/10.3891/acta.chem.scand.53-0076.
Full textTournier, Lucie, and Samir Z. Zard. "A practical variation on the Leuckart reaction." Tetrahedron Letters 46, no. 6 (2005): 971–73. http://dx.doi.org/10.1016/j.tetlet.2004.12.042.
Full textDai, Zengjin, Ying-Min Pan, Shou-Guo Wang, Xumu Zhang, and Qin Yin. "Direct reductive amination of ketones with ammonium salt catalysed by Cp*Ir(iii) complexes bearing an amidato ligand." Organic & Biomolecular Chemistry 19, no. 41 (2021): 8934–39. http://dx.doi.org/10.1039/d1ob01710a.
Full textM., L. SHARMA, K. TALWAR K., GUPTA ANU, and KISHORE LALIT. "Synthesis of Quaternary Salts of Ammonia from Aromatic Aldehydes via Leuckart Reaction and their Plant Growth Retardant Activity." Journal of Indian Chemical Society Vol. 74, Mar 1997 (1997): 233–34. https://doi.org/10.5281/zenodo.5889777.
Full textFrederick, Michael O., and Douglas P. Kjell. "A synthesis of abemaciclib utilizing a Leuckart–Wallach reaction." Tetrahedron Letters 56, no. 7 (2015): 949–51. http://dx.doi.org/10.1016/j.tetlet.2014.12.082.
Full textMaldonado, I. C. A. Romero, and G. A. Nikiforov. "Leuckart reaction for quinoid derivatives of 2,6-di-tert-butylphenol." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 10 (1987): 2184–85. http://dx.doi.org/10.1007/bf00962022.
Full textBannikov, G. F., G. A. Nikiforov, and V. V. Ershov. "Leuckart reaction of carbonyl derivatives of 2,6-di-tert-butylphenol." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 6 (1985): 1289–91. http://dx.doi.org/10.1007/bf00956104.
Full textAdger, Brian M., Ulrich C. Dyer, Ian C. Lennon, Peter D. Tiffin, and Simon E. Ward. "A novel synthesis of tert-leucine via a Leuckart type reaction." Tetrahedron Letters 38, no. 12 (1997): 2153–54. http://dx.doi.org/10.1016/s0040-4039(97)00269-4.
Full textBook chapters on the topic "Leuckart Reaction"
Li, Jie Jack. "Leuckart-Wallach reaction." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_174.
Full textLi, Jie Jack. "Leuckart–Wallach reaction." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_156.
Full textLi, Jie Jack. "Leuckart-Wallach reaction." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_163.
Full textLi, Jie Jack. "Leuckart–Wallach reaction." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_146.
Full textLi, Jie Jack. "Leuckart–Wallach Reaction." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_84.
Full textBlock, E. "Reductive Amination via the Leuckart Reaction." In Sulfur, Selenium, and Tellurium. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-039-00800.
Full textAustin, D. J., and S. M. Miller. "Reductive Amidation of Ketones (Leuckart Reaction)." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00073.
Full textUmar, Q., and M. Luo. "Recent Advances in the Syntheses of Amines with the Leuckart Reaction." In Novel Aspects on Chemistry and Biochemistry Vol. 5. B P International (a part of SCIENCEDOMAIN International), 2023. http://dx.doi.org/10.9734/bpi/nacb/v5/6089c.
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