ChemInform Abstract: Regioselective and Stereoselective Entry to β,β-Disubstituted Vinyl Ethers via the Sequential Hydroboration/Suzuki-Miyaura Coupling of Ynol Ethers.

ChemInform ◽  
2014 ◽  
Vol 45 (9) ◽  
pp. no-no
Author(s):  
Weijian Cui ◽  
Mengyi Mao ◽  
Zuying He ◽  
Gangguo Zhu
Keyword(s):  
Vinyl Ethers ◽  
Ynol Ethers

Pd-catalyzed addition of boronic acids to ynol ethers: a highly regio- and stereoselective synthesis of trisubstituted vinyl ethers

2013 ◽  
Vol 49 (69) ◽  
pp. 7650 ◽  
Author(s):  
Yihui Bai ◽  
Jing Yin ◽  
Wei Kong ◽  
Mengyi Mao ◽  
Gangguo Zhu
Keyword(s):  
Stereoselective Synthesis ◽  
Boronic Acids ◽  
Vinyl Ethers ◽  
Ynol Ethers

Vinyl Ethers

2021 ◽  
pp. 1-12
Author(s):  
Frank Bienewald ◽  
Pavel Tužina ◽  
Regina Vogelsang ◽  
Franz Ingo Berger ◽  
Sven Peter
Keyword(s):  
Vinyl Ethers

scholarly journals Stereodivergent approach in the protected glycal synthesis of L-vancosamine, L-saccharosamine, L-daunosamine and L-ristosamine involving a ring-closing metathesis step

2018 ◽  
Vol 14 ◽  
pp. 2949-2955 ◽  
Author(s):  
Pierre-Antoine Nocquet ◽  
Aurélie Macé ◽  
Frédéric Legros ◽  
Jacques Lebreton ◽  
Gilles Dujardin ◽  
...  
Keyword(s):  
Natural Products ◽  
Starting Material ◽  
Vinyl Ethers ◽  
Ring Closing Metathesis

In this paper, a new access to several chiral 3-aminoglycals as potential precursors for glycosylated natural products is reported from a common starting material, (−)-methyl-L-lactate. The stereodivergent strategy is based on the implementation of a ring-closing metathesis of vinyl ethers as key step of reaction sequences developed.

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