130633-06-6Relevant articles and documents
Practical synthesis of aromatic bisabolanes: Synthesis of 1,3,5-bisabolatrien-7-ol, peniciaculin A and B, and hydroxysydonic acid
Ishigami, Ken,Katsuta, Ryo,Murakawa, Hazuki,Saito, Tatsuo,Shiotani, Nanami,Shirakawa, Izumi,Ueda, Kazuya,Yajima, Arata
supporting information, (2021/06/12)
The enantioselective synthesis of aromatic bisabolanes, such as 1,3,5-bisabolatrien-7-ol, peniciaculin A and B, and hydroxysydonic acid, has been described. Our methodology for the total synthesis of aromatic bisabolanes involves the stereoselective const
NHC-catalyzed asymmetric α-regioselective [4 + 2] annulation to construct α-alkylidene-δ-lactones
Liu, Lala,Guo, Donghui,Wang, Jian
supporting information, p. 7025 - 7029 (2020/09/15)
The unprecedented NHC-catalyzed [4 + 2] annulation of α-bromoenals with dioxopyrrolidines is described. This protocol features broad substrate scope and allows rapid assembly of α-alkylidene-δ-lactones in good to high yields with excellent enantioselectivities. Notably, this process includes α-regioselective activation of azolium dienolate intermediates, which has not yet been reported.
Rh-Catalyzed Asymmetric Hydrogenation of β-Branched Enol Esters for the Synthesis of β-Chiral Primary Alcohols
Liu, Chong,Yuan, Jing,Zhang, Jian,Wang, Zhihui,Zhang, Zhenfeng,Zhang, Wanbin
supporting information, p. 108 - 111 (2018/01/17)
An asymmetric hydrogenation of β-branched enol esters has been developed for the first time, providing a new route for the synthesis of β-chiral primary alcohols. Using a (S)-SKP-Rh complex bearing a large bite angle and enol ester substrates possessing an O-fomyl directing group, the desired products were obtained in quantitative yields and with excellent enantioselectivities.