Stannyldienes, new tools for organic synthesis. preparatiom and reactivity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Synthesis of new lipoxygenase inhibitors 13-Thia- and 10-Thiaarachidonic acids
2. Regio- and stereoselective synthesis of trisubstituted vinylstannanes
3. Annulations leading to diene systems. Total synthesis of the diterpenoid (.+-.)-(14S)-dolasta-1(15),7,9-trien-14-ol
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1. Homoallenylboration of carbonyl compounds using inert 2-pinacolateboryl 1,3-butadienes via in situ generated borinic–TFA mixed anhydrides: efficient synthesis of homoallenyl alcohols;Organic Chemistry Frontiers;2023
2. The stannylvinyl cation that never was! New concentration- and temperature-dependent probe studies confirm an entirely free radical mechanism and O–Sn coordinative control of the hydrostannation of propargylically-oxygenated dialkyl acetylenes with stannanes and cat. Et3B;Tetrahedron;2020-05
3. Regioselective Synthesis of 2-Acylbutadienes from β,γ-Unsaturated Ketones;Synthesis;2019-07-15
4. The O‐Directed Free Radical Hydrostannation of Propargyloxy Dialkyl Acetylenes with Ph3SnH/cat. Et3B. A Refutal of the Stannylvinyl Cation Mechanism;The Chemical Record;2018-11-08
5. A Simple Procedure for the Synthesis of β ‐Hydroxyallenamides via Homoallenylation of Aldehydes;Advanced Synthesis & Catalysis;2018-02-20
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