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Efficient Generation of ortho-Quinone Methide: Application to the Biomimetic Syntheses of (±)-Schefflone and Tocopherol Trimers

https://doi.org/10.1021/ol202641y

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9783527634606openalex-snapshot

Biomimetic Organic Synthesis

inferredcites →https://doi.org/10.1002/anie.199102021openalex-snapshot

The Diels–Alder Dimer of 6‐Hydroxy‐2,6‐dimethyl‐ cyclohexa‐2,4‐dienone, an Unusual Metabolite in the Bacterial Degradation of 2,6‐Xylenol

inferredcites →https://doi.org/10.1002/jhet.232openalex-snapshot

Syntheses of chromenes and chromanes via o‐quinone methide intermediates

inferredcites →https://doi.org/10.1002/mrc.927openalex-snapshot

Determination of the absolute stereochemistry of vitamin E derived oxa‐spiro compounds by NMR spectroscopy

inferredcites →https://doi.org/10.1007/bf02536221openalex-snapshot

Formation of trimers of α‐tocopherol and its model compound, 2,2,5,7,8‐pentamethylchroman‐6‐ol, in autoxidizing methyl linoleate

inferredcites →https://doi.org/10.1007/s11418-009-0358-0openalex-snapshot

Hydroxyespintanol and schefflerichalcone: two new compounds from Uvaria scheffleri

inferredcites →https://doi.org/10.1007/s11745-001-0667-yopenalex-snapshot

Mechanisms of dimer and trimer formation from ultraviolet‐irradiated α‐tocopherol

inferredcites →https://doi.org/10.1016/0040-4020(77)80122-1openalex-snapshot

Quinones and quinone-methides—I

inferredcites →https://doi.org/10.1016/0040-4020(78)88036-3openalex-snapshot

Quinones and quinone methides—II

inferredcites →https://doi.org/10.1016/j.phytochem.2003.10.011openalex-snapshot

(±)-Schefflone: a trimeric monoterpenoid from the root bark of Uvaria scheffleri

inferredcites →https://doi.org/10.1016/j.tetlet.2006.07.113openalex-snapshot

A two-step biomimetic synthesis of antimalarial robustadials A and B

inferredcites →https://doi.org/10.1016/s0040-4020(01)85342-4openalex-snapshot

A short synthesis of the aromatic monoterpene espintanol

inferredcites →https://doi.org/10.1016/s0040-4020(02)00496-9openalex-snapshot

o-Quinone methides: intermediates underdeveloped and underutilized in organic synthesis

inferredcites →https://doi.org/10.1021/ja00874a025openalex-snapshot

The Oxidation Product from α-Tocopherol and Potassium Ferricyanide and Its Reaction with Ascorbic and Hydrochloric Acids

inferredcites →https://doi.org/10.1021/ja0120375openalex-snapshot

Flash Photolytic Generation of o-Quinone α-Phenylmethide and o-Quinone α-(p-Anisyl)methide in Aqueous Solution and Investigation of Their Reactions in that Medium. Saturation of Acid-Catalyzed Hydration

inferredcites →https://doi.org/10.1021/ja200356fopenalex-snapshot

Light-Induced Hetero-Diels−Alder Cycloaddition: A Facile and Selective Photoclick Reaction

inferredcites →https://doi.org/10.1021/ja205652mopenalex-snapshot

Patterned Surface Derivatization Using Diels–Alder Photoclick Reaction

inferredcites →https://doi.org/10.1021/ja803498ropenalex-snapshot

ortho-Quinone Methides from para-Quinones: Total Synthesis of Rubioncolin B

inferredcites →https://doi.org/10.1021/ja9031924openalex-snapshot

Photochemical Generation and the Reactivity ofo-Naphthoquinone Methides in Aqueous Solutions

inferredcites →https://doi.org/10.1021/ja905387ropenalex-snapshot

A Concise Synthesis of Berkelic Acid Inspired by Combining the Natural Products Spicifernin and Pulvilloric Acid

inferredcites →https://doi.org/10.1021/jo00828a038openalex-snapshot

Generation of O-quinone methides in solution. Trimerization

inferredcites →https://doi.org/10.1021/jo00836a016openalex-snapshot

O-quinone methides. II. Trapping with production of chromans

inferredcites →https://doi.org/10.1021/jo102531fopenalex-snapshot

Quinone Methide Generation via Photoinduced Electron Transfer

inferredcites →https://doi.org/10.1021/jo900504yopenalex-snapshot

Generation of ortho-Quinone Methides by p-TsOH on Silica and Their Hetero-Diels−Alder Reactions with Styrenes

inferredcites →https://doi.org/10.1021/jo960421sopenalex-snapshot

Concise Synthesis of Espintanol and Selected Regioisomeric Analogs

inferredcites →https://doi.org/10.1021/np070095jopenalex-snapshot

Cerebrosides and Tocopherol Trimers from the Seeds of Euryale ferox

inferredcites →https://doi.org/10.1021/np50074a015openalex-snapshot

Isolement et Synthese de l'Espintanol, Nouveau Monoterpene Antiparasitaire

inferredcites →https://doi.org/10.1021/ol100138kopenalex-snapshot

A Short Biomimetic Synthesis of the Meroterpenoids Guajadial and Psidial A

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Structural Reassignment of Cytosporolides A–C via Biomimetic Synthetic Studies and Reinterpretation of NMR Data

inferredcites →https://doi.org/10.1021/ol2022214openalex-snapshot

Total Synthesis and Repudiation of the Helianane Family

inferredcites →https://doi.org/10.1039/j39660002274openalex-snapshot

Oxidation of alkoxyphenols. Part VIII. Further examples of trimerisation to spiroketals

inferredcites →https://doi.org/10.1039/jr9540000243openalex-snapshot

Some products formed from phenolic inhibitors during the autoxidation of cumene

inferredcites →https://doi.org/10.1071/ch9780347openalex-snapshot

Quinones and quinone methides. III. A novel side-chain amination reaction of 2-(1-Phenylethyl)-1,4-benzoquinones

inferredcites →https://doi.org/10.1080/00304949609356526openalex-snapshot

EXPEDIENT SYNTHESES OF ESPINTANOL,p-METHOXYCARVACROL AND THYMOQUTNOL DIMETHYL ETHER

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ortho‐Quinone Methides in Natural Product Synthesis

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Self Cycloaddition of o‐Naphthoquinone Nitrosomethide to (±) Spiro{naphthalene(naphthopyranofurazan)}‐one Oxide: An Insight into its Formation

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Formation of Aza-ortho-quinone Methides Under Room Temperature Conditions: Cs2CO3 Effect

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