Items where authors include "Lichman, Benjamin R."

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Number of items: 17.

Article

Ingold, Zoe, Grogan, Gideon James orcid.org/0000-0003-1383-7056 and Lichman, Benjamin R. orcid.org/0000-0002-0033-1120 (2023) Structure and Mutation of Deoxypodophyllotoxin Synthase (DPS) from Podophyllum hexandrum. Frontiers in Catalysis. 1178345. ISSN 2673-7841

Kamileen, Mohamed O., Demars, Matthew D., Hong, Benke et al. (6 more authors) (2022) Recycling Upstream Redox Enzymes Expands the Regioselectivity of Cycloaddition in Pseudo-Aspidosperma Alkaloid Biosynthesis. Journal of the American Chemical Society. 19673–19679. ISSN 1520-5126

Hernández Lozada, Néstor J., Hong, Benke, Wood, Joshua C. et al. (10 more authors) (2022) Biocatalytic routes to stereo-divergent iridoids. Nature Communications. 4718. ISSN 2041-1723

Smit, Samuel J. orcid.org/0000-0002-7382-5113 and Lichman, Benjamin R. orcid.org/0000-0002-0033-1120 (2022) Plant biosynthetic gene clusters in the context of metabolic evolution. NATURAL PRODUCT REPORTS. ISSN 0265-0568

Rodríguez-López, Carlos E., Jiang, Yindi, Kamileen, Mohamed O. et al. (5 more authors) (2022) Phylogeny-Aware Chemoinformatic Analysis of Chemical Diversity in Lamiaceae Enables Iridoid Pathway Assembly and Discovery of Aucubin Synthase. Molecular Biology and Evolution. msac057. ISSN 0737-4038

Bat-Erdene, Undramaa, Billingsley, John M., Turner, William C. et al. (5 more authors) (2021) Cell-Free Total Biosynthesis of Plant Terpene Natural Products Using an Orthogonal Cofactor Regeneration System. ACS Catalysis. pp. 9898-9903. ISSN 2155-5435

Lichman, Benjamin R. orcid.org/0000-0002-0033-1120 (2021) The scaffold-forming steps of plant alkaloid biosynthesis. NATURAL PRODUCT REPORTS. pp. 103-129. ISSN 0265-0568

Eljounaidi, Kaouthar orcid.org/0000-0003-4675-226X and Lichman, Benjamin R. orcid.org/0000-0002-0033-1120 (2021) Dreaming of clean bean protein. Nature Plants. pp. 860-861. ISSN 2055-026X

Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, Godden, Grant T. and Buell, C. Robin (2020) Gene and genome duplications in the evolution of chemodiversity : perspectives from studies of Lamiaceae. CURRENT OPINION IN PLANT BIOLOGY. pp. 74-83. ISSN 1369-5266

Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, O'Connor, Sarah E. and Kries, Hajo (2019) Biocatalytic Strategies towards [4+2] Cycloadditions. Chemistry - A European Journal. pp. 6864-6877. ISSN 1521-3765

Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, Kamileen, Mohamed O., Titchiner, Gabriel R. et al. (4 more authors) (2018) Uncoupled activation and cyclization in catmint reductive terpenoid biosynthesis. NATURE CHEMICAL BIOLOGY. pp. 71-79. ISSN 1552-4450

Boachon, Benoît, Buell, C. Robin, Crisovan, Emily et al. (17 more authors) (2018) Phylogenomic Mining of the Mints Reveals Multiple Mechanisms Contributing to the Evolution of Chemical Diversity in Lamiaceae. Molecular plant. pp. 1084-1096. ISSN 1674-2052

Zhao, Jianxiong, Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, Ward, John M. et al. (1 more author) (2018) One-pot chemoenzymatic synthesis of trolline and tetrahydroisoquinoline analogues. Chemical Communications. pp. 1323-1326. ISSN 1364-548X

Wintle, Bonnie C., Boehm, Christian R., Rhodes, Catherine et al. (26 more authors) (2017) A transatlantic perspective on 20 emerging issues in biological engineering. eLife. e30247. ISSN 2050-084X

Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, Sula, Altin, Pesnot, Thomas et al. (3 more authors) (2017) Structural Evidence for the Dopamine-First Mechanism of Norcoclaurine Synthase. Biochemistry. pp. 5274-5277. ISSN 1520-4995

Erdmann, Vanessa, Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, Zhao, Jianxiong et al. (5 more authors) (2017) Enzymatic and Chemoenzymatic Three-Step Cascades for the Synthesis of Stereochemically Complementary Trisubstituted Tetrahydroisoquinolines. Angewandte Chemie - International Edition. pp. 12503-12507. ISSN 1433-7851

Lichman, Benjamin R. orcid.org/0000-0002-0033-1120, Zhao, Jianxiong, Hailes, Helen C. et al. (1 more author) (2017) Enzyme catalysed Pictet-Spengler formation of chiral 1,1'-disubstituted- and spiro-tetrahydroisoquinolines. Nature Communications. 14883. ISSN 2041-1723

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