Transition-Metal-Free Reductive Coupling of 1,3-Butadienes with Aldehydes Catalyzed by Dibutyliodotin Hydride
Author:
Affiliation:
1. Research Center for Environmental Preservation, Osaka University, 2-4 Yamadaoka, Suita, Osaka 565-0871, Japan
Funder
Naito Foundation
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02671
Reference30 articles.
1. Diastereoselective Allylation of Carbonyl Compounds and Imines: Application to the Synthesis of Natural Products
2. Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones
3. A New Catalytic CC Bond-Forming Hydrogenation: Reductive Coupling of Dienes and Glyoxals under Catalytic Hydrogenation Conditions
4. Iridium-Catalyzed C−C Coupling via Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level Employing 1,3-Cyclohexadiene
5. Ruthenium-Catalyzed C−C Bond Forming Transfer Hydrogenation: Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level Employing Acyclic 1,3-Dienes as Surrogates to Preformed Allyl Metal Reagents
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1. Reductive coupling of allenoates with aldehydes catalyzed by halogenotin hydride;Organic & Biomolecular Chemistry;2022
2. Direct use of 1,3-dienes for the allylation of ketones via catalytic hydroindation;RSC Advances;2020
3. Synthesis, Characterization and Antifungal Assessment of Optically Active Bis-organotin Compounds Derived from (S)-BINOL Diesters;Open Chemistry Journal;2019-05-31
4. Catalytic Annulation of Epoxides with Heterocumulenes by the Indium-Tin System;Molecules;2018-03-28
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