ChemInform Abstract: Synthesis of Ramirez Ylides from Morita-Baylis-Hillman Adducts of α-Bromocinnamaldehyde: An Intramolecular 1,6-Conjugate Addition of Phosphorus Ylide.

ChemInform ◽  
2015 ◽  
Vol 46 (44) ◽  
pp. no-no
Author(s):  
Ko Hoon Kim ◽  
Sangku Lee ◽  
Junseong Lee ◽  
Jae Nyoung Kim
2000 ◽  
Vol 166 (1) ◽  
pp. 99-109 ◽  
Author(s):  
Christopher D. Gabbutt ◽  
B. Mark Heron ◽  
Michael B. Hursthouse ◽  
K. M. Abdul Malik

2013 ◽  
Vol 13 (6) ◽  
pp. 802-813 ◽  
Author(s):  
Qun Qian ◽  
Zhenhua Zang ◽  
Yang Chen ◽  
Weiqi Tong ◽  
Hegui Gong

Molbank ◽  
10.3390/m1140 ◽  
2020 ◽  
Vol 2020 (2) ◽  
pp. M1140
Author(s):  
Jack Bennett ◽  
Paul Murphy

(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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