Topic
Selective reduction
About: Selective reduction is a research topic. Over the lifetime, 1394 publications have been published within this topic receiving 29090 citations. The topic is also known as: multifetal pregnancy reduction & Pregnancy Reduction, Multifetal.
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TL;DR: Aldehydes are reduced to alcohols with sodium formate in subcritical water at temperatures and pressures below those required to reduce cyclic ketones as mentioned in this paper, but they can afford only minor amounts of alcohol with Sodium formate even under more forcing conditions.
Abstract: Aldehydes are reduced to alcohols with sodium formate in subcritical water at temperatures and pressures below those required to reduce cyclic ketones. Acyclic ketones afford only minor amounts of alcohol with sodium formate even under more forcing conditions.
TL;DR: Cp. 2 YMe(THF) has been developed as an efficient catalyst for the selective reduction of substituted dienes as mentioned in this paper, which has been shown to be effective in the selective removal of substituted Dienes.
Abstract: Cp . 2 YMe(THF) has been developed as an efficient catalyst for the selective reduction of substituted dienes
TL;DR: In this paper, the reactivity of α-pinene was investigated in the reduction of carbonyl compounds, in the hope of better understanding the nature of the reagent and exploring its role in organic synthesis.
Abstract: ),an alicycloalkoxy derivative, examined its reactivity towardgeneral organic functional groups, and finally investigated itsselectivity in the reduction of carbonyl compounds, in thehope of better understanding the nature of the reagent andexploring its role in organic synthesis.The reagent was prepared from α-pinene by hydroborationfollowed by treatment with cyclohexanol in THF (Eq. 1).(1)The reactivity of Ipc
TL;DR: In this paper, the selective reduction of 2-(2-cyanopropyl)-4,5-dihydrooxazoles into heterocyclic amidines has been achieved with LAH in carefully controlled conditions.
Abstract: The selective reduction of 2-(2-cyanopropyl)-4,5-dihydrooxazoles into heterocyclic amidines has been achieved with LAH in carefully controlled conditions. This reaction was applied to the enantioselective synthesis of (S)-4-methylpyrrolidin-2-one, starting from (R)-phenylglycinol derived oxazoline 1b .