Pii: S0040-4020(00)00678-5
نویسندگان
چکیده
The diazo group of a series of a-diazo carbonyl compounds can be reduced to the corresponding CH2 group by Bu3SnH under Cu(acac)2-catalytic or photochemical conditions. The mechanistic aspects of this reaction were investigated in some detail, and a possible reaction pathway was discussed. q 2000 Elsevier Science Ltd. All rights reserved.
منابع مشابه
Pii: S0040-4020(00)00693-1
ÐKnoevenagel condensation between 3-nitro-2-pyridinecarbaldehyde and diethyl malonate catalyzed by titanium(IV) chloride gave diethyl 3-nitro-2-pyridylidenemalonate which was oxidized with peracetic acid to give corresponding 1-oxide. Reaction of the latter with diethylamine in the presence of primary and secondary alcohols resulted in the reduction of the nitro group and the oxidation of the v...
متن کاملPii: S0040-4020(97)00801-6
The synthesis of two classes of Philanthotoxin-343 analogs is described. Quantitative information on the antagonism of quisqualate-sensitive ionotropic glutamate receptors of insect muscle by these compounds is presented. © 1997 Elsevier Science Ltd.
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ÐTwo constrained analogs of the tripeptide hormone thyroliberin (TRH) have been synthesized. In both, the HisPro peptide bond of the hormone has been `locked' into a cis-conformation. In the ®rst analog, the constraint used was identical to the constraint used in an earlier trans-peptide bond analog that was a potent agonist for the TRH endocrine receptor TRH-R1. The second analog was built in ...
متن کاملPii: S0040-4020(97)10223-x
The nickel-catalyzed intramolecular cycloaddition of dienes with unactivatable alkynes is found to proceed under mild conditions while the corresponding Diels-Alder cycloaddition of the same substrates either fails or occurs only under forcing conditions. The nickel-catalyzed cycloaddition is also shown to occur with retention of stereochemistry and is not significantly influenced by electronic...
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