A New Annulation Based on a One-Pot Double Michael Addition Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH)

DOI: 10.1055/s-1997-793

Source and publish data:

Synlett p. 359 - 360 (1997)

Update date:2022-07-30

Topics:

Authors:

Saito, Susumu

Shiozawa, Masahito

Takamori, Yusuke

Yamamoto, Hisashi

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

Article abstract of DOI:10.1055/s-1997-793

An annulation system based on sequential inter- and intramolecular Michael addition was realized by the combined use of ketone enolates and aluminum tris(2,6-diphenylphenoxide)(ATPH).

Full text of DOI:10.1055/s-1997-793

Products guided by the article

Product name:Cyclohexanone, 4-acetyl-3-methyl-, trans- (9CI)

Cas No:143392-15-8

R&D Labs maybe for 143392-15-8

JADECHEM NINGBO CO.,LTD.

Contact:+86-574-89075960

Address:#100 Xiang Yun Road, New High tech area, Ningbo, China
Shanghai Xinda Pharmaceuticals Co., Ltd.

Contact:86-21-33692333-8008

Address:999 Linxian Road, Jinshan Industrial Park, Shanghai, China
JIANGXI ZHANGFENG CHEMICAL CO., LTD.

Contact:+86-0799-3413066

Address:Xiyuan village, Xiabu Town, Xiangdong District
Jiangsu Fengshan Group Co., Ltd.

Contact:86-25-86558671

Address:1903,Central International Mansion 105-6 North Zhongshan Road, Nanjing, China
Longhui qunfeng Chemical Co., Ltd

Contact:86-731-82173407

Address:South-east Industrial Park, Longhui County, Hunan Province, China

Relevant to this article

Transformation of 1-methyluracils and uridine to respective, 4-substituted pyrimidin-2(1H)-ones via pyridinium salts

Doi:10.1139/v92-113
(1992)
Mild oxidation of aldehydes to the corresponding carboxylic acids and esters: Alkaline iodine oxidation revisited

Doi:10.1016/S0040-4039(00)74252-3
(1992)
Doi:10.1002/hlca.19620450635
(1962)
A Simple Preparation of Five-Carbon Chiral Allylic and Homoallylic Alcohol Synthons

Doi:10.1055/s-1987-27863
(1987)
Generation of 1-aroxyisoquinolines via a silver-catalyzed reaction of 2-alkynylbenzaldoxime with phenol in the presence of p-toluenesulfonyl chloride

Doi:10.1016/j.tet.2013.04.076
(2013)
Regio- and enantioselective copper(I)-catalyzed hydroboration of borylalkenes: Asymmetric synthesis of 1,1-diborylalkanes

Doi:10.1002/anie.201208610
(2013)

Article Doi