Asymmetric synthesis of β-alkoxy substituted phenethylamide analogs

DOI: 10.1016/0040-4039(96)00465-0

Source and publish data:

Tetrahedron Letters p. 3045 - 3048 (1996)

Update date:2022-09-26

Topics:

Authors:

Zaponakis

Katerinopoulos

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0040-4039(96)00465-0

The enantioselective synthesis of beta-alkoxy substituted phenethylamines is described. The enantiomeric excess of the products ranges from 77 to 87%.

Full text of DOI:10.1016/0040-4039(96)00465-0

Products guided by the article

Product name:((S)-2-Chloro-1-phenyl-ethoxy)-trimethyl-silane

Cas No:177963-02-9

R&D Labs maybe for 177963-02-9

Zhejiang Tianyu Pharmaceutical Co., Ltd.

Contact:+86-576-84177669, 89189665,89189688,84168770

Address:Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang
Chengdu D-Innovation Pharmaceutical Co., Ltd

Contact:86-28-85105536

Address:1001, B6, No.88 Keyuan South Road, Chengdu Hi-Tech Zone
Shanghai FWD Chemicals ltd

website:http://www.fwdchem.com

Contact:86-21-54450828

Address:Room 802,Lotus Tower ,159 Tianzhou Road,Xuhui District,Shanghai
SINO Industries Company Limited(expird)

Contact:86-29-85369724

Address:No.111, Jiefang Road, Xi’an, China
Hebei Fulong Import & Export Co., Ltd.

Contact:86-311-87795661

Address:15A19 Zhongyuan Building,368 Youyi North Street,Shijiazhuang 050070,China

Relevant to this article

109. Oligosaccharide analogues of polysaccharides: Part 8. Orthogonally protected cellobiose-derived dialkynes. A convenient method for the regioselective bromo- and protodegermylation of trimethylgermyl- and trimethylsilyl-protected dialkynes

Doi:10.1002/hlca.19960790505
(1996)
Synthesis and biological evaluation of 4-alkoxy substituted trinems. Part 1

Doi:10.1016/0960-894X(96)00359-9
(1996)
Synthesis of some saccharin derivatives of expected biological activity based on n-(saccharinyl)-acetic acidazide

Doi:10.1080/10426509608046419
(1996)
Synthesis and nucleic-acid-binding properties of sulfamide- and 3′-N-sulfamate-modified DNA

Doi:10.1039/b110603c
(2002)
Biological activity and molecular docking studies of curcumin-related α,β-unsaturated carbonyl-based synthetic compounds as anticancer agents and mushroom tyrosinase inhibitors

Doi:10.1021/jf501145b
(2014)
Porphodilactones as synthetic chlorophylls: Relative orientation of ?-substituents on a Pyrrolic ring tunes NIR absorption

Doi:10.1021/ja502729x
(2014)

Article Doi