Reactions of Triethylaluminum with α,β-Unsaturated Carbonyl Compounds
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چکیده
منابع مشابه
AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with various α,β-unsaturated carbonyl compounds under mild conditions are described, which provides a facile and efficient pathway for the synthesis of 1-alkylated isoquinoline derivatives. The method tolerates a wide range of substrates and allows for the preparation of the products of interest in moderate to excellent yields.
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ome of the most useful reactions of carbonyl compounds involve carbonhydrogen bonds adjacent to the carbonyl group. Such reactions, which can be regarded as the backbone of much synthetic organic chemistry, usually result in the replacement of the hydrogen by some other atom or group, as in the I I I I sequence H-C-C=O -+ X-C-C=O. The important examples we I I will consider in this chapter are ...
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Technical iodine was found to catalyze the condensation between 2-aminobenzohydrazide (1) and some aldehydes and ketones in absolute ethanol under mild conditions to afford hydrazone and quinazoline derivatives, respectively. Condensation of 1 with terephthalaldehyde (2) in 1 : 1 molar ratios afforded the hydrazone 3, while hydrazone 4 was formed on using a double molar ratio of 1. On the other...
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Reactions of a neutral silyleneruthenium complex with ketones and aldehydes, and isolation of their agostic intermediates are reported, where an alpha-H abstraction or hydrosilylation of the carbonyl compounds occurs depending on the substituents of the substrates.
متن کاملSynthesis of 3,4-Dihydro-2/f-pyrans by Hetero-Diels-Alder Reactions of Functionalized a,/?-Unsaturated Carbonyl Compounds with Styrenes
H etero-Diels-Alder Reaction, a,/?-Unsaturated Ketones, Styrenes Cycloadditions of 3-aryl-2-benzoyl-2-propenenitriles la,b to styrene (2a) and its methylor methoxy-substituted derivatives 2b-d proceed regioand diastereoselectively yielding cis and trans diastereoisomers of 2,4,6-triaryl-3,4-dihydro-2//-pyran-5-carbonitriles 3 and 4 in 59-72% yield. Cycloadducts cis-3 were the major products. Re...
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1968
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.41.928