A novel synthetic method for optically active terpenes by the ring-opening reaction of (R)-(+)-β-methyl-β-propiolactone
T Sato, T Kawara, A Nishizawa, T Fujisawa
Index: Tetrahedron Letters, , vol. 21, p. 3377 - 3380
Full Text: HTML
Citation Number: 66
Abstract
... Tetrahedron Letters. Volume 21, Issue 35, 1980, Pages 3377–3380. ... Optically active terpene such as (R)-(+)citronellol, (R)-(+)pulegone or (S)-ar-turmerone is prepared in high enantiomeric excess from an intermediate, (R)-(+)citronellic acid or (S)-(+)3-p-tolylbutyric acid ...
Related Articles:
[Shimizu, Hideo; Nagano, Takuto; Sayo, Noboru; Saito, Takao; Ohshima, Takashi; Mashima, Kazushi Synlett, 2009 , # 19 p. 3143 - 3146]
Mo (CO) 6-promoted facile deoxygenation of α, β-epoxy ketones and α, β-epoxy esters
[Patra, Asit; Bandyopadhyay, Mausumi; Mal, Dipakranjan Tetrahedron Letters, 2003 , vol. 44, # 11 p. 2355 - 2357]
[Chemistry - A European Journal, , vol. 14, # 7 p. 2060 - 2066]
[Murahashi, Shun-Ichi; Sasao, Shigehiro; Saito, Eiichiro; Naota, Takeshi Tetrahedron, 1993 , vol. 49, # 39 p. 8805 - 8826]
[Chemistry - A European Journal, , vol. 14, # 7 p. 2060 - 2066]