Sentence examples for coupling partner in from inspiring English sources

Exact(3)

Note that, by using PhOH- d5 as coupling partner in the absence of D2O, we did not observe any deuterium scrambling (Scheme 5).

Nearly simultaneously to the publication of our report on the redox arylation, the group of Jana published a very similar strategy, employing fluorenone as a coupling partner in place of an aldehyde.

The same group reported the direct arylation of benzo[ b]furan with chloropyrazines.[ 13b] The most C2 selective protocol was reported by Doucet and co-workers just recently.[ 11h] By using benzylsulfonyl chlorides as coupling partner in combination with [PdCl2(MeCN 2] and Li2CO3, they were able to arylate benzo[ b]furan selectively at C2 in generally good yields (13 examples, 50 91 %).

Similar(57)

Synthesis of vinyl iodide 84 by this method was advantageous since both (E -vinyl iodidE -vinyl (E)-viodidetannane 84 could be used andcoupling partnE -vinylhE -vinyl reaction (stannane16).

Mori et al. used iodobenzene, 4-iodoanisol, and ethyl 4-iodobenzoate as coupling partners in the direct arylation of benzo[ b]furan.[ 10a] For iodobenzene, no isolated yield was reported, only an NMR yield of 41%% and with no further comments.

38, 39 During attempts to use 3-furanyl boronic acid (11) as a cross-coupling partner in reactions with L1, we observed full conversion but obtained only 30%% product formation and 70%% deiodinated starting material.

Justices of the peace were advised to use words like "companions" and "partners" to describe the couples and to pronounce the couples "partners in life" or "partners for life," Ms. Loglisci said.

Biomathematical calculations have shown that prosthetic instability can be reduced by regarding stem and cup as coupled partners in a biomechanical system [ 6].

After establishing suitable reaction conditions for the amination of 1a with morpholine (2), we probed the use of other 1-naphthyl-based electrophilic coupling partners 1 in this methodology (Table 2).

For the first time, alkenylzinc reagents were suitable coupling partners, delivering 46b in 94% yield and 91% ee.

Several aryl pyrazole coupling partners were prepared in this way, and could be reacted with intermediates such as 4 or 5 to provide the target compounds (see Table 2).

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