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Efficient O-Acylation of Alcohols and Phenol Using Cp<sub>2</sub>TiCl as a Reaction Promoter.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 21, p. 3584, doi. 10.1002/ejoc.201600496
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- Article
Unexpected Mild Protection of Alcohols as 2- O-THF and 2- O-THP Ethers Catalysed by Cp<sub>2</sub>TiCl Reveal an Intriguing Role of the Solvent in the Single-Electron Transfer Reaction.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 28, p. 6333, doi. 10.1002/ejoc.201500869
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Handbook of Biotransformations of Aromatic Compounds. By Brian L. Goodwin.
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- ChemBioChem, 2005, v. 6, n. 5, p. 928, doi. 10.1002/cbic.200500128
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<sup>13</sup>C NMR spectra of some trichothecene mycotoxins and derivatives.
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- Magnetic Resonance in Chemistry, 1988, v. 26, n. 6, p. 475, doi. 10.1002/mrc.1260260608
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- Article
Römpp encyclopedia of natural products W. Steglich, B. Fugmann and S. Lang-Fugmann (eds) Georg Thieme Verlag, Stuttgart, 2000 x + 748 pages. DM 498 ISBN 3-13-117711-X.
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- Applied Organometallic Chemistry, 2001, v. 15, n. 5, p. 440, doi. 10.1002/aoc.151
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- Article
Natural products from the hallucinogenic sage.
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- Science Progress, 2010, v. 93, n. 2, p. 171, doi. 10.3184/003685010X12626983776947
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The chemistry of the bio-control agent, Trichoderma harzianum.
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- Science Progress, 2005, v. 88, n. 4, p. 237, doi. 10.3184/003685005783238372
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A hundred years in the elucidation of the structures of natural products.
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- Science Progress, 2017, v. 100, n. 1, p. 63, doi. 10.3184/003685017X14876775256129
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Some contributions of organic chemistry to the study of the biosynthesis of natural products.
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- Science Progress, 2017, v. 100, n. 2, p. 194, doi. 10.3184/003685017X14901006155071
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From Caá-ehé to a commercial sweetener – the diterpenoid glycosides of Stevia rebaudiana.
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- Science Progress, 2016, v. 99, n. 4, p. 413, doi. 10.3184/003685016X14773090197508
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From 'mad honey' to hypotensive agents, the grayanoid diterpenes.
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- Science Progress, 2016, v. 99, n. 3, p. 327, doi. 10.3184/003685016X14720691270831
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- Article
Rosemary, the beneficial chemistry of a garden herb.
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- Science Progress, 2016, v. 99, n. 1, p. 83, doi. 10.3184/003685016X14495646283298
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Foreword to the special feature on Sir John Cornforth.
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- Science Progress, 2015, v. 98, n. 3, p. 211, doi. 10.3184/003685015X14383592079434
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Sir John Cornforth AC CBE FRS: his synthetic work.
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- Science Progress, 2015, v. 98, n. 3, p. 219, doi. 10.3184/003685015X14364588807198
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Sir John and Lady Rita Cornforth: a distinguished chemical partnership.
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- Science Progress, 2015, v. 98, n. 3, p. 212, doi. 10.3184/003685015X14364530625058
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Current strategies for the elucidation of the structures of natural products.
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- Science Progress, 2015, v. 98, n. 2, p. 177, doi. 10.3184/003685015X14308420934112
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- Article
Sir John Cornforth AC CBE FRS: his biosynthetic work.
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- Science Progress, 2015, v. 98, n. 3, p. 230, doi. 10.3184/003685015X14365489399849
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- Article
Microbiological hydroxylations with Cephalosporium aphidicola.
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- Journal of Chemical Research, 2018, v. 42, n. 10, p. 498, doi. 10.3184/174751918X15380407503010
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Aphidicolin: Its chemistry and biosynthesis.
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- Journal of Chemical Research, 2018, v. 42, n. 8, p. 395, doi. 10.3184/174751918X15333061990467
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Stereochemical aspects of some rearrangements of gibberellic acid.
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- Journal of Chemical Research, 2018, v. 42, n. 6, p. 285, doi. 10.3184/174751918X15294211268538
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Skeletal rearrangements of rings C and D of the kaurene and beyerene tetracyclic diterpenoids.
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- Journal of Chemical Research, 2018, v. 42, n. 4, p. 175, doi. 10.3184/174751918X15233039624478
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Stereochemical aspects of the hydrogenolysis of derivatives of terpenoid and steroidal allylic alcohols.
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- Journal of Chemical Research, 2018, v. 42, n. 1, p. 1, doi. 10.3184/174751918X15161933697763
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The ozonolysis of terpenoids, a Pandora's box of by-products.
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- Journal of Chemical Research, 2017, v. 41, n. 10, p. 557, doi. 10.3184/174751917X15064232103029
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Pseudo-natural products, some artefacts formed during the isolation of terpenoids.
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- Journal of Chemical Research, 2017, v. 41, n. 9, p. 497, doi. 10.3184/174751917X15021050367558
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The botryane sesquiterpenoid metabolism of the fungus Botrytis cinerea.
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- Journal of Chemical Research, 2017, v. 41, n. 8, p. 435, doi. 10.3184/174751917X14993374065962
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Exploiting a step in diterpenoid biosynthesis by the fungus Fusarium fujikuroi.
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- Journal of Chemical Research, 2017, v. 41, n. 2, p. 65, doi. 10.3184/174751917X14850069001130
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Some recent reports on the flavonoids.
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- Journal of Chemical Research, 2016, v. 40, n. 1, p. 62, doi. 10.3184/174751916X14502778885176
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Recent advances in the chemistry of the terpenoids.
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- Journal of Chemical Research, 2015, v. 39, n. 12, p. 738, doi. 10.3184/174751915X14453508186023
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Chiral cyclic synthetic intermediates from readily available monoterpenoids.
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- Journal of Chemical Research, 2015, v. 39, n. 12, p. 677, doi. 10.3184/174751915X14471674408987
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Chiral acylic synthetic intermediates from readily available monoterpenoids.
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- Journal of Chemical Research, 2015, v. 39, n. 11, p. 617, doi. 10.3184/174751915X14444964546522
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The aromatisation of terpenes and steroids by dehydrogenation.
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- Journal of Chemical Research, 2015, v. 39, n. 3, p. 127, doi. 10.3184/174751915X14246963094093
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The chemistry of B-norsteroidal 6-ketones and their relatives.
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- Journal of Chemical Research, 2011, v. 35, n. 9, p. 495, doi. 10.3184/174751911X13146264913491
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The reactions of B-norsteroidal 4- and 5-enes.
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- Journal of Chemical Research, 2009, v. 2009, n. 12, p. 713, doi. 10.3184/030823409X12573626050671
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