Deracemization via highly enantioselective enolate protonation using a chiral aniline as the "acid"

DOI: 10.1021/ja00084a080

Source and publish data:

Journal of the American Chemical Society p. 2175 - 2176 (1994)

Update date:2022-08-05

Topics:

Authors:

Vedejs Vedejs

Lee Lee

Sakata Sakata

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

Article abstract of DOI:10.1021/ja00084a080

Full text of DOI:10.1021/ja00084a080

Products guided by the article

Product name:(R)-N,N-diisopropyl-2-(cyclohex-1-en-3-yl)propionamide

Cas No:155680-49-2

R&D Labs maybe for 155680-49-2

Josun International Limited

website:http://www.josunpharma.com

Contact:+86-311-80715268 80766839

Address:No.39, Zhaiying Street, Shijaizhuang,Hebei,China
Suzhou Chiral Pharmaceuticals Co., Ltd.

Contact:86-0512-63197058

Address:Building A, No. 2358, Chang'an Road, Wujiang Science Park
Wuhan Better Organic Technology Inc.

Contact:13307163183

Address:Wuhan Economic&Technology Development Zone, Hubei
ABA Chemicals (Shanghai) Limited

Contact:021- 5115 9199-232

Address:Suite 18D, #201 Ningxia Road,
Shanghai Bojing Chemical Co., Ltd.

Contact:021-37122233

Address:6F Buildiing 11,No.388,Baifu Road,District Fengxian.Shanghai, China.

Relevant to this article

Synthesis of pentasaccharide core structures corresponding to the genus-specific lipolysaccharide epitope of Chlamydia

Doi:10.1016/0008-6215(94)84246-9
(1994)
Retinobenzoic Acids. 6. Retinoid Antagonists with a Heterocyclic Ring

Doi:10.1021/jm00036a017
(1994)
Synthesis of 2-pyrrolyl complexes of ruthenium and osmium via hydrolysis of a chloro(pyrrolyl)carbene ligand or via transmetalation reactions using (2-pyrrolyl)mercuric chloride

Doi:10.1021/om00019a009
(1994)
Copper-mediated sequential C-N and N-N bond formation: Facile synthesis of symmetrical 1,2,4-triazoles

Doi:10.1055/s-0033-1338985
(2013)
Intramolecular [4 + 2] trapping of a hexadehydro-diels-alder (HDDA) benzyne by tethered arenes

Doi:10.1021/ol5037024
(2015)
Construction of polyaromatics via photocyclization of 2-(fur-3-yl) ethenylarenes, using a 3-furyl group as an isopropenyl equivalent synthon

Doi:10.1016/j.tet.2014.01.035
(2014)

Article Doi