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  2. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    The Buchner ring expansion reaction was first used in 1885 by Eduard Buchner and Theodor Curtius [2] [3] who prepared a carbene from ethyl diazoacetate for addition to benzene using both thermal and photochemical pathways in the synthesis of cycloheptatriene derivatives. The resulting product was a mixture of four isomeric carboxylic acids ...

  3. Büchner funnel - Wikipedia

    en.wikipedia.org/wiki/Büchner_funnel

    It is commonly thought to be named after the Nobel Laureate Eduard Buchner (without umlaut), but it is actually named after the industrial chemist Ernst Büchner. [2] A Büchner funnel fitted with Sintered Disc made of Boro 3.3 Glass. Diagram of filtration set-up using a Büchner flask

  4. Ring expansion and contraction - Wikipedia

    en.wikipedia.org/wiki/Ring_expansion_and_contraction

    A generalized mechanism of the Buchner ring expansion. A common method for expanding a ring involves opening cyclopropane-containing bicyclic intermediate. The strategy can start with a Simmons-Smith-like cyclopropanation of a cyclic alkene. [3] A related cyclopropane-based ring expansion is the Buchner ring expansion.

  5. Dropping funnel - Wikipedia

    en.wikipedia.org/wiki/Dropping_funnel

    cylindrical type graduated and ungraduated with cone and socket; with pressure equalizing tube; pear shaped, graduated and ungraduated; Pressure-equalizing dropping funnels have an additional narrow-bore glass tube from the bulb of the funnel, to the ground glass joint around the stem.

  6. Büchner flask - Wikipedia

    en.wikipedia.org/wiki/Büchner_flask

    The short tube and hose barb effectively act as an adapter over which the end of a thick-walled flexible hose (tubing) can be fitted to form a connection to the flask.

  7. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    The Buchner–Curtius–Schlotterbeck reaction is the reaction of aldehydes or ketones with aliphatic diazoalkanes to form homologated ketones. [1] It was first described by Eduard Buchner and Theodor Curtius in 1885 [ 2 ] and later by Fritz Schlotterbeck in 1907. [ 3 ]

  8. Berlese funnel - Wikipedia

    en.wikipedia.org/wiki/Berlese_funnel

    [3] Another variation uses naphthalene flakes or similar aromatic mothballs in place of a heat source to drive organisms downward. [ 4 ] This method finds application in situations without electrical power, where the organisms are repulsed by volatile preservatives in collection container, or they cannot migrate downward quickly enough to avoid ...

  9. Ernst Büchner - Wikipedia

    en.wikipedia.org/wiki/Ernst_Büchner

    His father was the pharmacist, chemist, industrialist and politician Wilhelm Büchner.Ernst was also the nephew of the playwright Georg Büchner and the philosopher, physiologist and physician Ludwig Büchner.