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Datta Gopal K..
High stereoselectivity in chelation-controlled intermolecular Heck reactions with aryl chlorides, vinyl chlorides and vinyl triflates
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Organic & Biomolecular Chemistry, 2008
[PubMed: 18264566]
[DOI: 10.1039/b719131f]
Jana N; Nguyen Q; Driver TG.
Development of a Suzuki cross-coupling reaction between 2-azidoarylboronic pinacolate esters and vinyl triflates to enable the synthesis of [2,3]-fused indole heterocycles.
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The Journal of organic chemistry
[PubMed: 24571492]
[DOI: 10.1021/jo500252e]
Willis MC; Claverie CK; Mahon MF.
Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling.
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Chemical communications (Cambridge, England)
G?ndisch D; Harms K; Schwarz S; Seitz G; Stubbs MT; Wegge T.
Synthesis and evaluation of diazine containing bioisosteres of (-)-ferruginine as ligands for nicotinic acetylcholine receptors.
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Bioorganic & medicinal chemistry
Padilla-Salinas R; Walvoord RR; Tcyrulnikov S; Kozlowski MC.
Nitroethylation of vinyl triflates and bromides.
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Organic letters
[DOI: 10.1021/ol401747u]
Okutani M; Mori Y.
Synthesis of alkynes from vinyl triflates using tetrabutylammonium fluoride.
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Chemical & pharmaceutical bulletin
[DOI: 10.1248/cpb.c15-00146]
Al-huniti MH; Lepore SD.
Zinc(II) catalyzed conversion of alkynes to vinyl triflates in the presence of silyl triflates.
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Organic letters
[DOI: 10.1021/ol501852n]
Liao L; Jana R; Urkalan KB; Sigman MS.
A palladium-catalyzed three-component cross-coupling of conjugated dienes or terminal alkenes with vinyl triflates and boronic acids.
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Journal of the American Chemical Society
[DOI: 10.1021/ja201358b]
Moreira VM; Salvador JA; Sim?es S; Destro F; Gavioli R.
Novel oleanolic vinyl boronates: synthesis and antitumor activity.
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European journal of medicinal chemistry
[DOI: 10.1016/j.ejmech.2013.01.040]
Beaulieu ED; Voss L; Trauner D.
Conjugate addition of allyl stannanes with concomitant triflation.
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Organic letters
[DOI: 10.1021/ol702996t]
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