Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes
Author:
Affiliation:
1. Max-Planck-Institut für Kohlenforschung; 45470 Mülheim/Ruhr Germany
Funder
Max-Planck-Gesellschaft
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Reference136 articles.
1. On the Stereospecific Conversion of Proximally-Oxygenated Trisubstituted Vinyltriphenylstannanes into Stereodefined Trisubstituted Alkenes
2. Asymmetric Total Synthesis of (+)-Inthomycin C via O-Directed Free Radical Alkyne Hydrostannation with Ph3SnH and Catalytic Et3B: Reinstatement of the Zeeck–Taylor (3R)-Structure for (+)-Inthomycin C
3. Synthesis of the C(7)–C(22) Sector of (+)-Acutiphycin via O-Directed Double Free Radical Alkyne Hydrostannation with Ph3SnH/Et3B, Double I–Sn Exchange, and Double Stille Coupling
4. Enantioselective formal total synthesis of the Dendrobatidae frog toxin, (+)-pumiliotoxin B, via O-directed alkyne free radical hydrostannation
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