Buchler GmbH
  • Products
    • Active Pharmaceutical Ingredients
    • Asymmetric Synthesis
      • Chiral Building Blocks
      • Chiral Phase Transfer Catalysts (PTCs)
      • Chiral Screening Kit
      • Enantioselective Organocatalysts
      • Racemic Resolution
    • Food Ingredients
    • Product Overview
  • Chiral Catalyst Search
  • Contact
  • About
    • Certificates
    • Company Policy
    • Former Buchler Company Managers
    • Galleries
      • Gallery current production and storage
      • Gallery Laboratory
      • Gallery Historical Production
    • History of Buchler
  • Career
Select Page

Strecker Synthesis, N-(4-nitrobenzyl)-3-phenylpropanimidoyl cyanide, (E)-but-2-enal, α,α-dialkyl aminonitriles, 9-[(6-chloro-2,5-diphenyl-4-pyrimidinyl)oxy]-1-[[2′-(1,1-dimethylethoxy)-3,3′′,4,4′′,5,5′′-hexamethoxy[1,1′:3′,1′′-terphenyl]-5′-yl]methyl]-6′-methoxy-cinchonanium bromide, Quinidine Derivative

Strecker

Michael Addition, 4-methoxybenzyl 2-bromo-3-(ethylthio)-3-oxopropanoate, (E)-(2-nitrovinyl)benzene, 4-methoxybenzyl (2S,3R)-2-bromo-2-((ethylthio)carbonyl)-4-nitro-3-phenylbutanoate, S-ethyl (1R,2R,3R)-2-nitro-3-phenylcyclopropane-1-carbothioate, 3-[[[3,5-bis(trifluoromethyl)phenyl]methyl]amino]-4-[[(9R)-6′-methoxycinchonan-9-yl]amino]-3-Cyclobutene-1,2-dione, Quinidine Derivative

Cyclopropanation, Michael, Michael Addition

Spirocyclization, 1-benzyl-5-bromoindoline-2,3-dione, malononitrile, benzo[d][1,3]dioxol-5-ol, spiro[4H-chromene-3,3′-oxindoles], 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(9R)-6′-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione, Quinidine Derivative

Cascade reaction, Spirocyclization

Vinylogous Michael addition, β-acyl acrylates, 1,2-diacylethylenes, α,β-unsaturated γ-butyrolactam, substituted (R)-2-((R)-5-oxo-2,5-dihydro-1H-pyrrol-2-yl)succinaldehyde, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxycinchonan-9-yl]thiourea, Quinidine Derivative

Michael Addition, Vinylogous Michael Addition

Spirocyclization, isatins, γ-hydroxy enones, cyclic acetals with spirooxindole skeleton, 3-[[(8α,9S)-6′-methoxycinchonan-9-yl]amino]-4-(tricyclo[3.3.1.13,7]dec-1-ylamino)-3-cyclobutene-1,2-dione, Quinine Derivative

Spirocyclization

Peroxidation, α,β-unsaturated aldehydes, peroxides, β-peroxid aldehydes, (9R)-6′-methoxy-cinchonan-9-amine, Quinidine Derivative

Further reactions, Peroxidation

Decarboxylative Protonation, substituted meldrum’s acid, tert-butyl hydroxy((phenylsulfonyl)methyl)carbamate, tert-butyl (R)-4-benzyl-5-oxoisoxazolidine-2-carboxylate, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxycinchonan-9-yl]thiourea, Quinidine Derivative

Decarboxylative Protonation, Protonation

Phospha-Michael, diphenyl phosphonate, nitroalkenes, β-nitrophosphonates, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxycinchonan-9-yl]thiourea, Quinidine Derivative

Michael Addition, Phospha-Michael Addition

Alkylation, arenesulfonylalkylindoles, 1,3-diketones, 3-sec-alkyl-substituted indoles, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxycinchonan-9-yl]thiourea, Quinidine Derivative

Alkylation, alpha-Alkylation

Aza-Diels-Alder, (E)-4-(4-methylstyryl)benzo[e][1,2,3]oxathiazine 2,2-dioxide, interrupted cyclic 2,5‐dienones, trienamines, (9R)-6′-methoxy-cinchonan-9-amine, Quinidine Derivative

Cycloaddition, Diels-Alder reaction

« Older Entries
Next Entries »

Glossary

Impressum / Legal Notice

Code of Conduct

Hinweisgebersystem / Whistleblowing System

Allgemeine Geschäfts-bedingungen / General Terms and Conditions

Datenschutzhinweise / Data Protection Information

Contact

My Account
  • Follow
  • Follow

All Rights Reserved by Buchler GmbH