Regiocontrolled 1,2-, 1,4-, and 1,6-additions of organometallics to unsaturated thioamides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. 1,4-Addition reaction of organolithium and -magnesium compounds to .alpha.,.beta.-unsaturated thioamides
2. 1,4-Addition reactions of lithium enolates to .alpha.,.beta.-unsaturated thioamides
3. Stereoselective generation of Z-enolates of thioamides: its application to diastereoselective aldol condensations and thio-Claisen rearrangements
4. Action des organomagnesiens allyliques sur quelques thiocetones cyclisation de thiols β,γ-ethyleniques
5. Conjugate Additions of Grignard Reagents to alpha, beta- Unsaturated Esters. IX. 1,4- and 1,6-Additions of n-Butylmagnesium Bromide to the sec-Butyl Ester of Sorbic Acid.
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1. Reductive Functionalization of Carboxamides: A Recent Update;Bulletin of the Chemical Society of Japan;2020-11-15
2. Transition‐Metal‐Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α‐Branched Amine Synthesis;Angewandte Chemie International Edition;2020-05-18
3. Transition‐Metal‐Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α‐Branched Amine Synthesis;Angewandte Chemie;2020-05-18
4. Iridium‐Catalyzed Reductive Coupling of Grignard Reagents and Tertiary Amides;Organic Syntheses;2020-04-29
5. Iridium-Catalyzed Reductive Coupling of Grignard Reagents and Tertiary Amides;Organic Syntheses;2019
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