Octet

Octet / Reagents

Diethyl Tartrate (DET)

Diethyl Tartrate (DET) (C₈H₁₄O₆) - catalyst reagent. Chiral ligand for asymmetric synthesis. Common uses: Sharpless asymmetric epoxidation, D-(-)-DET and L-(+)-DET control enantioselectivity. D-tartrate: "draws" from right. L-tartrate: "draws" from left (mnem...

Catalyst

Reagent details

Name

Diethyl Tartrate (DET)

Formula

C₈H₁₄O₆

Category

Catalyst

Function

Chiral ligand for asymmetric synthesis

Common Uses

  1. Sharpless asymmetric epoxidation

  2. D-(-)-DET and L-(+)-DET control enantioselectivity

Notes

D-tartrate: "draws" from right. L-tartrate: "draws" from left (mnemonic).

This is one row of the Reagent guide sheet - print all 63 reagents on one page.

Reagents

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Sodium Borohydride

Sodium Borohydride (NaBH₄) - reducing reagent. Mild reduction of aldehydes and ketones to alcohols. Common uses: Aldehyde → Primary alcohol, Ketone → Secondary alcohol. Does NOT reduce esters, amides, carboxylic acids, or C=C bonds. Works in protic solvents (...

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Lithium Aluminum Hydride

Lithium Aluminum Hydride (LiAlH₄) - reducing reagent. Strong reduction of most carbonyl compounds. Common uses: Aldehyde → Primary alcohol, Ketone → Secondary alcohol, Ester → Two alcohols, Carboxylic acid → Primary alcohol, Amide → Amine, Nitrile → Primary a...

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DIBAL-H

DIBAL-H ((i-Bu)₂AlH) - reducing reagent. Partial reduction of esters to aldehydes. Common uses: Ester → Aldehyde (at -78°C), Nitrile → Aldehyde (via imine). Temperature critical! At -78°C stops at aldehyde. Warmer or excess gives alcohol.

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H₂/Pd (Catalytic Hydrogenation)

H₂/Pd (Catalytic Hydrogenation) (H₂ + Pd/C) - reducing reagent. Reduction of C=C, C≡C, and some functional groups. Common uses: Alkene → Alkane, Alkyne → Alkane, Nitro → Amine (ArNO₂ → ArNH₂), Benzyl groups removed (hydrogenolysis). Syn addition. Also works w...

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Lindlar Catalyst

Lindlar Catalyst (Pd/CaCO₃/Pb) - reducing reagent. Partial reduction of alkynes to cis-alkenes. Common uses: Alkyne → cis-Alkene (stops at alkene). Poisoned catalyst - lead prevents over-reduction. Syn addition gives cis product.

Reducing

Dissolving Metal (Na/NH₃)

Dissolving Metal (Na/NH₃) (Na + NH₃(l)) - reducing reagent. Reduction of alkynes to trans-alkenes. Common uses: Alkyne → trans-Alkene. Birch reduction conditions. Liquid ammonia at -33°C. Radical mechanism gives trans product.

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