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  2. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Download as PDF; Printable version; ... In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined. Cross-couplings are a ...

  3. Crossover experiment (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Crossover_experiment...

    Crossover experiments allow for experimental study of a reaction mechanism. Mechanistic studies are of interest to theoretical and experimental chemists for a variety of reasons including prediction of stereochemical outcomes, optimization of reaction conditions for rate and selectivity, and design of improved catalysts for better turnover number, robustness, etc. [6] [7] Since a mechanism ...

  4. Two-dimensional nuclear magnetic resonance spectroscopy

    en.wikipedia.org/wiki/Two-dimensional_nuclear...

    The key feature of a COSY spectrum is the presence of cross-peaks as shown in Figure 1, indicating coupling between pairs of nuclei. These cross-peaks provide crucial information about the connectivity within a molecule, showing that the two nuclei are connected by a small number of bonds, usually two or three bonds.

  5. Cross-cutting relationships - Wikipedia

    en.wikipedia.org/wiki/Cross-cutting_relationships

    Cross-cutting relationships can be used to determine the relative ages of rock strata and other structures. Explanations: A – folded rock strata cut by a thrust fault; B – large intrusion (cutting through A); C – erosional angular unconformity (cutting off A & B) on which rock strata were deposited; D – volcanic dike (cutting through A, B & C); E – even younger rock strata (overlying ...

  6. List of restriction enzyme cutting sites: A - Wikipedia

    en.wikipedia.org/wiki/List_of_restriction_enzyme...

    Recognition sequence: Sequence of DNA recognized by the enzyme and to which it specifically binds. Cut: Displays the cut site and pattern and products of the cut. The recognition sequence and the cut site usually match, but sometimes the cut site can be dozens of nucleotides away from the recognition site. [5] [6]

  7. Fukuyama coupling - Wikipedia

    en.wikipedia.org/wiki/Fukuyama_coupling

    Although the Fukuyama cross-coupling reaction has been widely used in natural product synthesis, the reaction mechanism remains unclear.Various catalysts have been shown to promote reactivity, including Pd/C, Pd(OH) 2 /C, Pd(OAc) 2, PdCl 2, NiCl 2, Ni(acac) 2, etc. [2] The proposed catalytic cycle using Pd(OH) 2 /C (Pearlman’s catalyst) features the in situ generation of active Pd/C by ...

  8. R.EcoRII - Wikipedia

    en.wikipedia.org/wiki/R.EcoRII

    EcoRII is a bacterial Type IIE [2] REase that interacts with two [3] or three [4] copies of the pseudopalindromic DNA recognition sequence 5'-CCWGG-3' (W = A or T), one being the actual target of cleavage, the other(s) serving as the allosteric activator(s). EcoRII cuts the target DNA sequence CCWGG, generating sticky ends. [5]

  9. Cross-coupling partner - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_partner

    In cross-coupling reactions, the component reagents are called cross-coupling partners or simply coupling partners. These reagents can be further classified according to their nucleophilic vs electrophilic character: R-X + R'-Y → R-R' + XY. Typically the electrophilic coupling partner (R-X) is an aryl halide, but triflates are also used ...