Solubility Measurement and Correlation of (+)-Biotin Intermediate Lactone in Different Organic Solvents from 287.15 to 323.75 K
Author:
Affiliation:
1. Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, Zhejiang, 310027, P. R. China
Funder
Ministry of Education of the People's Republic of China
National Natural Science Foundation of China
Zhejiang Provincial Public Technology Research of China
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jced.5b00857
Reference23 articles.
1. Goldberg, M. W.; Stembach, L. H.Synthesis of Biotin. U.S. Patent 2,489,232, November 22, 1949.
2. Goldberg, M. W.; Stembach, L. H.Synthesis of Biotin. U.S. Patent 2,489,235, November 22, 1949.
3. Goldberg, M. W.; Stembach, L. H.Debenzylation of Benzylated Imidazolido-Thiophane Compounds. U.S. Patent 2,489,238, November 22, 1949.
4. Versuche zur Biotinsynthese. Herstellung von (3aS, 6aR)-1, 3-Dibenzyl-tetrahydro-4H-thieno[3, 4-d]imidazol-2,4(1H)-dion
5. Synthetic Studies ond-Biotin, Part 8:[1] An Efficient Chemoenzymatic Approach to the Asymmetric Total Synthesis ofd-Biotinvia a Polymer-Supported PLE-Mediated Desymmetrization ofmeso-Symmetic Dicarboxylic Esters
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