Organocatalytic Asymmetric Conjugate Addition to Allenic Esters and Ketones

2008 ◽  
Vol 130 (14) ◽  
pp. 4897-4905 ◽  
Author(s):  
Petteri Elsner ◽  
Luca Bernardi ◽  
Giorgio Dela Salla ◽  
Jacob Overgaard ◽  
Karl Anker Jørgensen
Keyword(s):  
Conjugate Addition ◽  
Allenic Esters

Stereoselective formation of tertiary and quaternary carbon centers via inverse conjugate addition of carbonucleophiles to allenic esters

Tetrahedron ◽  
2010 ◽  
Vol 66 (39) ◽  
pp. 7720-7725 ◽  
Author(s):  
Ana Lúcia Cardoso ◽  
Ana Matos Beja ◽  
Manuela Ramos Silva ◽  
Jesús M. de los Santos ◽  
Francisco Palacios ◽  
...  
Keyword(s):  
Conjugate Addition ◽  
Quaternary Carbon ◽  
Carbon Centers ◽  
Allenic Esters

Phosphine-Catalyzed β-Selective Conjugate Addition of α-Fluoro-β-ketoamides to Allenic Esters

2019 ◽  
Vol 2019 (35) ◽  
pp. 6138-6142
Author(s):  
Narendra Kumar Vaishanv ◽  
Mohd Khalid Zaheer ◽  
Ruchir Kant ◽  
Kishor Mohanan
Keyword(s):  
Conjugate Addition ◽  
Allenic Esters

ChemInform Abstract: Organocatalytic Asymmetric Conjugate Addition to Allenic Esters and Ketones

ChemInform ◽  
2008 ◽  
Vol 39 (33) ◽  
Author(s):  
Petteri Elsner ◽  
Luca Bernardi ◽  
Giorgio Dela Salla ◽  
Jacob Overgaard ◽  
Karl Anker Joergensen
Keyword(s):  
Conjugate Addition ◽  
Allenic Esters

Fluoride-Mediated α-Selective 1,6-Conjugate Addition of Allenic Esters to p-Quinone Methides

2018 ◽  
Vol 83 (15) ◽  
pp. 8759-8767 ◽  
Author(s):  
Narendra Kumar Vaishanv ◽  
Ashis Kumar Gupta ◽  
Ruchir Kant ◽  
Kishor Mohanan
Keyword(s):  
Conjugate Addition ◽  
Quinone Methides ◽  
Allenic Esters

Nickel and Cobalt-Catalyzed Coupling of Alkyl Halides with Alkenes via Heck Reactions and Radical Conjugate Addition

2013 ◽  
Vol 13 (6) ◽  
pp. 802-813 ◽  
Author(s):  
Qun Qian ◽  
Zhenhua Zang ◽  
Yang Chen ◽  
Weiqi Tong ◽  
Hegui Gong
Keyword(s):  
Conjugate Addition ◽  
Alkyl Halides ◽  
Heck Reactions

scholarly journals (2S,3R,6R)-2-[(R)-1-Hydroxyallyl]-4,4-dimethoxy-6-methyltetrahydro-2H-pyran-3-ol

Molbank ◽  
10.3390/m1140 ◽  
2020 ◽  
Vol 2020 (2) ◽  
pp. M1140
Author(s):  
Jack Bennett ◽  
Paul Murphy
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
Ir Spectroscopy ◽  
13C Nmr ◽  
Conjugate Addition ◽  
13C Nmr Spectroscopy ◽  
One Pot ◽  
1H And 13C Nmr ◽  
Esi Mass Spectrometry ◽  
The One

(2S,3R,6R)-2-[(R)-1-Hydroxyallyl]-4,4-dimethoxy-6-methyltetrahydro-2H-pyran-3-ol was isolated in 18% after treating the glucose derived (5R,6S,7R)-5,6,7-tris[(triethylsilyl)oxy]nona-1,8-dien-4-one with (1S)-(+)-10-camphorsulfonic acid (CSA). The one-pot formation of the title compound involved triethylsilyl (TES) removal, alkene isomerization, intramolecular conjugate addition and ketal formation. The compound was characterized by 1H and 13C NMR spectroscopy, ESI mass spectrometry and IR spectroscopy. NMR spectroscopy was used to establish the product structure, including the conformation of its tetrahydropyran ring.

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