James R. Hanson

Affiliations: 
University of Sussex, Falmer, England, United Kingdom 
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"James R. Hanson"
Bio:

(1937-2018)
https://doi.org/10.1039/C9NP90032B

Mean distance: 8.09
 
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Publications

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Moraga J, Gomes W, Pinedo C, et al. (2019) The current status on secondary metabolites produced by plant pathogenic Colletotrichum species Phytochemistry Reviews. 18: 215-239
Suárez I, da Silva Lima G, Conti R, et al. (2018) Structural and biosynthetic studies on eremophilenols related to the phytoalexin capsidiol, produced by Botrytis cinerea. Phytochemistry. 154: 10-18
Izquierdo-Bueno I, Moraga J, Cardoza RE, et al. (2018) Relevance of the deletion of the Tatri4 gene in the secondary metabolome of Trichoderma arundinaceum. Organic & Biomolecular Chemistry
Botubol-Ares JM, Durán-Peña MJ, Hanson JR, et al. (2018) Cp2Ti(III)Cl and Analogues as Sustainable Templates in Organic Synthesis Synthesis. 50: 2163-2180
Botubol-Ares JM, Hanson JR, Hernández-Galán R, et al. (2017) Mild Epoxidation of Allylic Alcohols Catalyzed by Titanium(III) Complexes: Selectivity and Mechanism. Acs Omega. 2: 3083-3090
Franco Dos Santos G, Moraga J, Takahashi JA, et al. (2017) The formation of sesquiterpenoid presilphiperfolane and cameroonane metabolites in the Bcbot4 null mutant of Botrytis cinerea. Organic & Biomolecular Chemistry
Collado IG, Hanson JR, Sanchez AJM. (2017) The botryane sesquiterpenoid metabolism of the fungus Botrytis cinerea Journal of Chemical Research-S. 41: 435-440
Durán-Peña MJ, Botubol-Ares JM, Hanson JR, et al. (2016) Efficient O-Acylation of Alcohols and Phenol Using Cp2TiCl as a Reaction Promoter. European Journal of Organic Chemistry. 2016: 3584-3591
Moraga J, Dalmais B, Izquierdo-Bueno I, et al. (2016) Genetic and molecular basis of botrydial biosynthesis. Connecting cytochrome P450-encoding genes to biosynthetic intermediates. Acs Chemical Biology
Pinedo C, Moraga J, Barua J, et al. (2016) Chemically-induced cryptic sesquiterpenoids and expression of sesquiterpene cyclases in Botrytis cinerea revealed new sporogenic (+)-4-epieremophil-9-en-11-ols. Acs Chemical Biology
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