Chemistry Letters p. 221 - 224 (1986)
Update date:2022-07-29
Topics: Conjugate addition Diastereomers Silyl enol ether Trityl perchlorate Aldol addition Tetrahydropyran Trifluoroacetic acid Triethylsilane Facile Method Stereoselective Syntheses
Kobayashi, Shu
Mukaiyama, Teruaki
In the presence of a catalytic amount of trityl perchlorate, the intermediate adducts, produced in situ by the conjugate addition of silyl enol ethers with α,β-unsaturated ketones, react with aldehydes to give the corresponding γ-acyl substituted δ-hydrox
View MoreContact:86-551-63540590
Address:No 1388 Furong Rd., Hefei, Anhui, China
Engineering Research Center of Pesticide, Heilongjiang Province
Contact:+86-451-86609001
Address:No.74 of Xuefu Road, Nangang District,
Reliable Pharma Technology (Shanghai) Co., Ltd.
Contact:0086-21-67676847-8008
Address:Lane 1500, No.68, Xinfei Road, Songjiang District, Shanghai, 201611, P.R.China.
Shanghai PengMo Biotechnology Co.,Ltd
website:http://www.pengmobio.lookchem.com
Contact:86-13052359378
Address:No.218 Hai Qu Road.Shanghai.China
TAIZHOU XINGCHENG CHEMPHARM CO.,LTD.
Contact:0086-0576-88551200,88886292 ,88880039
Address:B Area. 10 Floor.Yaodadasha. 289#.Shifu Road.Taizhou.Zhejiang.China
Doi:10.1021/ol801747m
(2008)Doi:10.1002/chem.202101602
(2021)Doi:10.1039/jr9360000587
(1936)Doi:10.1039/b803067g
(2008)Doi:10.1016/j.jorganchem.2008.05.043
(2008)Doi:10.1021/ja01154a066
(1951)
