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Collect. Czech. Chem. Commun. 1998, 63, 525-533
https://doi.org/10.1135/cccc19980525

Enantioselective Preparation of the Stereoisomersof 4-Methylheptan-3-ol Using Candida antarctica Lipase B

C. Rikard Unelius, Johan Sandell and Christian Orrenius

Department of Chemistry, Organic Chemistry, Royal Institute of Technology, SE-100 44 Stockholm, Sweden

Crossref Cited-by Linking

  • Lv Jia-Xiang, Ding Ya-Qi, Huang Chen-Ming, Guo Ling-Ling, Fang Jia-Li, Jia Xian, Zhang Wen-He, You Song, Qin Bin: Enzyme- and Chemo-enzyme-Catalyzed Stereodivergent Synthesis. Pharmaceutical Fronts 2022, 04, e121. <https://doi.org/10.1055/s-0042-1755556>
  • Brenna Elisabetta, Crotti Michele, Gatti Francesco, Monti Daniela, Parmeggiani Fabio, Pugliese Andrea: One-Pot Multi-Enzymatic Synthesis of the Four Stereoisomers of 4-Methylheptan-3-ol. Molecules 2017, 22, 1591. <https://doi.org/10.3390/molecules22101591>
  • Unelius C. R., Park K.-C., McNeill M., Wee S. L., Bohman B., Suckling D. M.: Identification and electrophysiological studies of (4S,5S)-5-hydroxy-4-methyl-3-heptanone and 4-methyl-3,5-heptanedione in male lucerne weevils. Naturwissenschaften 2013, 100, 135. <https://doi.org/10.1007/s00114-012-1003-4>
  • Anderbrant Olle, Matteson Donald S., Unelius C. Rikard, Pharazyn Philip S., Santangelo Ellen M., Schlyter Fredrik, Birgersson Göran: Pheromone of the elm bark beetle Scolytus laevis (Coleoptera: Scolytidae): stereoisomers of 4-methyl-3-heptanol reduce interspecific competition. Chemoecology 2010, 20, 179. <https://doi.org/10.1007/s00049-010-0042-6>
  • Larsson Michael, Andersson Jimmy, Liu Rong, Högberg Hans-Erik: Enantiopure building blocks for the synthesis of 3-methyl-2-alkanols. Diastereoselective methylmetal addition to a chiral 2-methylaldehyde followed by lipase catalysed esterification. Tetrahedron: Asymmetry 2004, 15, 2907. <https://doi.org/10.1016/j.tetasy.2004.07.049>
  • Růžička Josef, Koutek Bohumı́r, Streinz Ludvı́k, Šaman David, Lešetický Ladislav: A new access to β-methyl substituted secondary alcohols. Application to the synthesis of 4-methylheptan-3-ol. Tetrahedron: Asymmetry 1999, 10, 3521. <https://doi.org/10.1016/S0957-4166(99)00372-9>
  • UNELIUS C. R., SANDELL J., ORRENIUS C.: ChemInform Abstract: Enantioselective Preparation of the Stereoisomers of 4‐Methylheptan‐3‐ol Using Candida antarctica Lipase B. ChemInform 1998, 29. <https://doi.org/10.1002/chin.199837277>