Deprotonation of Chelating Enamines. Direct Formation of β-Lithio Enamines

DOI: 10.1021/ja00262a025

Source and publish data:

Journal of the American Chemical Society p. 304 - 305 (1986)

Update date:2022-08-04

Topics:

Authors:

Stork, Gilbert

Shiner, Christopher S.

Cheng, Chi-Wen

Polt, Robin L.

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

Article abstract of DOI:10.1021/ja00262a025

Full text of DOI:10.1021/ja00262a025

Products guided by the article

Product name:C₁₁H₂₁⁽²⁾HN₂

Cas No:102839-35-0

R&D Labs maybe for 102839-35-0

Jinan Baozhao Pharmaceutical Co., Ltd

Contact:0086-531-86397156 82371858 82371868

Address:Huaneng Road, Jinan, Shandong ,China
changsha chenjin chemical technology co.,LtD(expird)

Contact:86-731-84451263

Address:Room 201/217-218, 101 Jingyuan Electronic Technology Co.,Ltd. Testing Center, No.69, Lufeng Road, High-tech Development Zone, Changsha, China
Jiangxi Sunway Chemical Co. Ltd.

Contact:86-794-5259909

Address:Zone C Industry Park Jinxi
Changzhou Sunlight Pharmaceutical Co., Ltd.

Contact:+86-519-83131668;83139028;83138042;83137041

Address:JiuliStreet, Benniu Town Changzhou City, Jiangsu Province
Anyang Double Circle Auxiliary CO.,LTD

Contact:0086-134 6082 4403

Address:dongfeng road, anyang city, henan province,china

Relevant to this article

REACTION OF ALKYNYLTRIMETHYLSILANES WITH A HYPERVALENT ORGANOIODINE COMPOUND: A NEW GENERAL SYNTHESIS OF ALKYNYLIODONIUM SALTS

Doi:10.1016/S0040-4039(00)88941-8
(1985)
Visible Light-Mediated (Hetero)aryl Amination Using Ni(II) Salts and Photoredox Catalysis in Flow: A Synthesis of Tetracaine

Doi:10.1021/acs.joc.9b03107
(2020)
Doi:10.1021/ja01476a024
(1961)
1,3-Dipolar cycloadditions of N-benzyl-2,3-O-isopropylidene-D- glyceraldehyde nitrone to methoxyallene - Control of site- and diastereoselectivity of isoxazolidine formation by Lewis acids

Doi:10.1002/ejoc.200700724
(2008)
Doi:10.1021/jo01106a041
(1958)
Chiral bisphosphine ligands based on quinoline oligoamide foldamers: application in asymmetric hydrogenation

Doi:10.1039/c9ob01649j
(2019)

Article Doi