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  2. Tetrahydrofuran - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrofuran

    Tetrahydrofuran (THF), or oxolane, is an organic compound with the formula (CH 2) 4 O. The compound is classified as heterocyclic compound , specifically a cyclic ether . It is a colorless, water- miscible organic liquid with low viscosity .

  3. Tetrahydro-2-furoic acid - Wikipedia

    en.wikipedia.org/wiki/Tetrahydro-2-furoic_acid

    Reaction of tetrahydro-2-furoic acid with the hydrochloride salt of 3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino]-propanenitrile provided alfuzosin, a drug for the treatment of benign prostatic hyperplasia (BPH).

  4. Tetrahydrofolic acid - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrofolic_acid

    Tetrahydrofolic acid is a cofactor in many reactions, especially in the synthesis (or anabolism) of amino acids and nucleic acids.In addition, it serves as a carrier molecule for single-carbon moieties, that is, groups containing one carbon atom e.g. methyl, methylene, methenyl, formyl, or formimino.

  5. Transition metal ether complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_ether_complex

    Common ether ligands are diethyl ether and tetrahydrofuran. Common chelating ether ligands include the glymes, dimethoxyethane (dme) and diglyme, and the crown ethers. Being lipophilic, metal-ether complexes often exhibit solubility in organic solvents, a property of interest in synthetic chemistry.

  6. Lithium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Lithium_naphthalene

    In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. Lithium naphthalene crystallizes with ligands bound to Li +. [1] The anion is a well-known example of an organic radical.

  7. Hydroboration–oxidation reaction - Wikipedia

    en.wikipedia.org/wiki/Hydroboration–oxidation...

    Hydroboration–oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol. [1] The process results in the syn addition of a hydrogen and a hydroxyl group where the double bond had been.

  8. 2-Methyltetrahydrofuran - Wikipedia

    en.wikipedia.org/wiki/2-Methyltetrahydrofuran

    2-Methyltetrahydrofuran (2-MeTHF) is an organic compound with the molecular formula C 5 H 10 O. It is a highly flammable, mobile liquid. It is mainly used as a replacement for Tetrahydrofuran (THF) in specialized applications for its better performance, such as to obtain higher reaction temperatures, or easier separations (as, unlike THF, it is not miscible with water).

  9. 3-Hydroxytetrahydrofuran - Wikipedia

    en.wikipedia.org/wiki/3-Hydroxytetrahydrofuran

    Additionally, 3-OH THF has been an intermediate to developmental drug substances, such as chemotherapy agents. For example, reaction of phosphorus pentasulfide with 3-hydroxytetrahydrofuran has been used in the synthesis of bis(O,O-di(tetrahydrofuran-3-yl)hydrogen dithiophosphate)platinum(II), a cisplatin analog.