SynStrategy categorizes 500 reactions by the functional group they form. It is completely free for iOS: rb.gy/wl8aym and Android: rb.gy/yf2xn0

Joined September 2022
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The newest update to @SynStrategy is live, bringing a top requested feature: a quiz function! Save reactions to custom datasets and test your knowledge across 3 quiz or flashcard formats. Check it out! iOS: apps.apple.com/de/app/synstr… Android: play.google.com/store/apps/d… #ChemTwitter
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In SynStrategy, you can build custom datasets, like a curated list of asymmetric reactions, and quiz yourself in multiple formats. Here is a look at the Advanced mode: Do you know the name of this reaction used in the #TotalSynthesis of ( )-clerocidin?
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The Keck allylation employs catalytic Ti(OiPr)4 and BINOL to enantioselectively allylate aldehydes and access homoallylic alcohols. The #reaction was applied in the #TotalSynthesis of (-)-Mandelalide A by the Altmann group @ETH_DCHAB References in thread!
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The Brown asymmetric allylation/crotylation employs diisopinocampheylborane for the enantio- and diastereoselective synthesis of homoallylic alcohols. The #reaction was applied by the Denmark group @ChemistryUIUC in the #TotalSynthesis of ( )-Brasilenyne. References in thread!
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The Petasis-Ferrier #rearrangement transforms vinyl acetals into β-hydroxy ketones in the presence of a Lewis acid. Cyclic substrates result in tetrahydropyranones, a strategy applied in the #TotalSynthesis of (-)-Okilactomycin by the Smith group. Links in thread!
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In the Davis asymmetric oxidation, a chiral oxaziridine derived from camphorsulfonic acid enables the enantioselective α-hydroxylation of enolates. The Holton group leveraged this #Reaction in the first #TotalSynthesis of #Taxol. Links in thread!
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The Arndt-Eistert homologation proceeds via a ketene intermediate to transform acid chlorides or anhydrides into homologated carboxylic acids, esters, or amides. This method was utilized in the #TotalSynthesis of ( )-Jasplakinolide by the Grieco group. Links in thread!
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The Semmler-Wolff #Reaction transforms α,β-unsaturated oximes into aniline derivatives under acidic conditions or heat. This transformation was applied in the #TotalSynthesis of (-)-Penitrem D by the Smith group. Links in thread!
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The Achmatowicz reaction transforms a furyl alcohol into a dihydropyranone via an oxidative rearrangement using Br₂, NBS, or mCPBA. This transformation was applied in the #TotalSynthesis of (±)-Tirandamycin by the DeShong group. Links in thread!
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Link to the #TotalSynthesis of (±)-Tirandamycin: pubs.acs.org/doi/abs/10.1021… Explore more reactions and their synthetic applications and download the app! iOS: apps.apple.com/de/app/synstr… Android: play.google.com/store/apps/d…
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The Marshall propargylation is a palladium-catalyzed stereoselective addition of a propargyl group to an aldehyde, affording homopropargylic alcohols. This method was utilized in the #TotalSynthesis of ( )-Neaumycin B by the Wang, Zhang, and Chen groups. Links in thread!
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The [2,3]-Wittig rearrangement can occur when allylic ethers are treated with a strong base, transforming them into homoallylic alcohols. An application was reported by the Ding Group in the #TotalSynthesis of ( )-Vulgarisin B. Links in thread!
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The Ohira-Bestmann reagent transforms aldehydes into terminal alkynes under mild conditions. A notable application was reported by the Wender group ( @StanfordUChem ) in their #TotalSynthesis of (-)-Laulimalide. Links in thread!
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