Relevant bibliographies by topics / Hydrolytic kinetic resolution (HKR)

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  1. Journal articles

Academic literature on the topic 'Hydrolytic kinetic resolution (HKR)'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Hydrolytic kinetic resolution (HKR)"

1

Krishna, Palakodety, Mopuri Reddy, and Gembali Manikanta. "First Stereoselective Total Synthesis of Anti-Inflammatory Metabolite­ Penicillinolide A." Synthesis 51, no. 06 (2018): 1427–34. http://dx.doi.org/10.1055/s-0037-1611040.

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The first asymmetric total synthesis of penicillinolide A is described. Key steps of the synthesis involve Jacobsen’s hydrolytic kinetic resolution (HKR), chelation controlled allylation, Brown’s asymmetric allylation, hydroboration, and Yamaguchi lactonization.
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2

Pemha, René, Dieudonné Emmanuel Pegnyemb, and Paul Mosset. "Synthesis of (2S,3R,5R)-2-Azido-3,5-dihydroxynonadecane Sphingolipid Analogue." Synthesis 52, no. 17 (2020): 2572–78. http://dx.doi.org/10.1055/s-0040-1707397.

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A concise and highly efficient synthesis of an enigmol analogue has been achieved. The synthetic strategy features Jacobsen’s hydrolytic kinetic resolution (HKR) and epoxide opening by alkynyl boranes as the key steps.
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3

Kumar, Pradeep, Vasudeva Naidu, and Priti Gupta. "Application of hydrolytic kinetic resolution (HKR) in the synthesis of bioactive compounds." Tetrahedron 63, no. 13 (2007): 2745–85. http://dx.doi.org/10.1016/j.tet.2006.12.015.

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4

Yang, Yun-Xu, and Shi-Xiang Liu. "Asymmetric-Catalysed Preparation and Stereochemistry of (R,R)-,(S,R)-(6-Fluoro-2-Chromanyl)-1,2-Ethanediol." Journal of Chemical Research 2007, no. 9 (2007): 506–8. http://dx.doi.org/10.3184/030823407x240908.

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(R,R)-,(S,R)-1-(6-fluoro-2-chromanyl)-1,2-ethanediol 1a/1b were prepared by hydrolytic kinetic resolution (HKR) of terminal racemic epoxides using (R,R)-SalenCo(OAc) as a catalyst. Their configurations were established by comparison with two authentic samples by HPLC.
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5

Kureshy, R. I., N. H. Khan, S. H. R. Abdi, S. T. Patel, and R. V. Jasra. "Simultaneous production of chirally enriched epoxides and 1,2-diols from racemic epoxides via hydrolytic kinetic resolution (HKR)." Journal of Molecular Catalysis A: Chemical 179, no. 1-2 (2002): 73–77. http://dx.doi.org/10.1016/s1381-1169(01)00394-6.

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6

Rossbach, Benjamin M., Kerstin Leopold, and Ralf Weberskirch. "Self-Assembled Nanoreactors as Highly Active Catalysts in the Hydrolytic Kinetic Resolution (HKR) of Epoxides in Water." Angewandte Chemie International Edition 45, no. 8 (2006): 1309–12. http://dx.doi.org/10.1002/anie.200503291.

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7

Aerts, Sven, Anita Buekenhoudt, Herman Weyten, Ivo F. J. Vankelecom, and Pierre A. Jacobs. "The influence of solvent choice, acid activation and surfactant addition on the hydrolytic kinetic resolution (HKR) of terminal epoxides." Tetrahedron: Asymmetry 16, no. 3 (2005): 657–60. http://dx.doi.org/10.1016/j.tetasy.2004.11.024.

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8

Roy, Tamal, Sunirmal Barik, Manish Kumar, et al. "Asymmetric hydrolytic kinetic resolution with recyclable polymeric Co(iii)–salen complexes: a practical strategy in the preparation of (S)-metoprolol, (S)-toliprolol and (S)-alprenolol: computational rationale for enantioselectivity." Catal. Sci. Technol. 4, no. 11 (2014): 3899–908. http://dx.doi.org/10.1039/c4cy00594e.

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9

Aerts, S., A. Buekenhoudt, H. Weyten, L. E. M. Gevers, I. F. J. Vankelecom, and P. A. Jacobs. "The use of solvent resistant nanofiltration in the recycling of the Co-Jacobsen catalyst in the hydrolytic kinetic resolution (HKR) of epoxides." Journal of Membrane Science 280, no. 1-2 (2006): 245–52. http://dx.doi.org/10.1016/j.memsci.2006.01.025.

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10

Key, Rebecca E., Krishnan Venkatasubbaiah, and Christopher W. Jones. "Evaluation of enantiopure and non-enantiopure Co(III)-salen catalysts and their counter-ion effects in the hydrolytic kinetic resolution (HKR) of racemic epichlorohydrin." Journal of Molecular Catalysis A: Chemical 366 (January 2013): 1–7. http://dx.doi.org/10.1016/j.molcata.2012.08.013.

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