Highly(≥98%) Selective Trisubstituted Alkene Synthesis of Wide Applicability via Fluoride-Promoted Pd-Catalyzed Cross-Coupling of Alkenylboranes
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Highly selective synthesis of conjugated dienoic and trienoic esters via alkyne elementometalation-Pd-catalyzed cross-couplingHighly(≥98%) Stereo- and Regioselective Trisubstituted Alkene Synthesis of Wide Applicability via 1-Halo-1-alkyne Hydroboration-Tandem Negishi-Suzuki Coupling or Organoborate Migratory Insertion Protocol.Search for highly efficient, stereoselective, and practical synthesis of complex organic compounds of medicinal importance as exemplified by the synthesis of the C21-C37 fragment of amphotericin B.A regio- and stereoselective synthesis of trisubstituted alkenes via gold(I)-catalyzed hydrophosphoryloxylation of haloalkynes.Stereo- and Regiocontrolled Methylboration of Terminal Alkynes.Synthesis of the Conjugated Tetraene Acid Side Chain of Mycolactone E by Suzuki-Miyaura Cross-Coupling Reaction of Alkenyl Boronates
P2860
Highly(≥98%) Selective Trisubstituted Alkene Synthesis of Wide Applicability via Fluoride-Promoted Pd-Catalyzed Cross-Coupling of Alkenylboranes
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on December 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Highly(≥98%) Selective Trisubs ...... oss-Coupling of Alkenylboranes
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type
label
Highly(≥98%) Selective Trisubs ...... oss-Coupling of Alkenylboranes
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prefLabel
Highly(≥98%) Selective Trisubs ...... oss-Coupling of Alkenylboranes
@en
P2093
P2860
P356
P1476
Highly(≥98%) Selective Trisubs ...... oss-Coupling of Alkenylboranes
@en
P2093
Ching-Tien Lee
Ei-Ichi Negishi
Honghua Rao
Shiqing Xu
Tomas Tobrman
P2860
P304
P356
10.1002/IJCH.201000051
P577
2010-12-01T00:00:00Z