diisopropylethylamine

diisopropylethylamine
диизопропилэтиламин

English-Russian names of organic compounds . 2015.

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  • N,N-diisopropyléthylamine — Structure de la diisopropyléthylamine Général Nom IUPAC N éthyl N propan 2 ylpropan 2 amine …   Wikipédia en Français

  • N,N-Diisopropylethylamine — IUPAC name Ethyldiisopropylamine …   Wikipedia

  • DIEA — diisopropylethylamine …   Medical dictionary

  • DIEA — • diisopropylethylamine …   Dictionary of medical acronyms & abbreviations

  • Sonogashira coupling — In organic chemistry, a Sonogashira coupling is a coupling reaction of terminal alkynes with aryl or vinyl halides. This reaction was first reported by Kenkichi Sonogashira and Nobue Hagihara in 1975. [cite journal author = K. Sonogashira, Y.… …   Wikipedia

  • Wender Taxol total synthesis — starting from a naturally occurring compound with ring construction in the order A,B,C,D. The Wender effort is shorter by approximately 10 steps. Raw materials for the preparation of Taxol by this route include verbenone, prenyl bromine, allyl… …   Wikipedia

  • Swern oxidation — The Swern oxidation, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol is oxidized to an aldehyde or ketone using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine. [cite… …   Wikipedia

  • Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

  • Peptide synthesis — In organic chemistry, peptide synthesis is the production of peptides, which are organic compounds in which multiple amino acids are linked via peptide bonds which are also known as amide bonds. The biological process of producing long peptides… …   Wikipedia

  • Triethylamine — Triethylamine …   Wikipedia

  • Azide alkyne Huisgen cycloaddition — The Azide Alkyne Huisgen Cycloaddition is a 1,3 dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3 triazole. Rolf Huisgen[1] was the first to understand the scope of this organic reaction. American chemist K …   Wikipedia


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