On the reaction of Meldrum's acid with N- trimethylsilylanilines substituted by electron withdrawing groups

DOI: 10.1002/jhet.5570360439

Source and publish data:

Journal of Heterocyclic Chemistry p. 1073 - 1075 (1999)

Update date:2022-08-04

Topics:

Authors:

Roche, Sandrine

Yous, Said

Couturier, Daniel

Rigo, Benoit

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

Article abstract of DOI:10.1002/jhet.5570360439

The reaction of Meldrum's acid with silylated anilines substituted by an electron withdrawing group easily yields the corresponding N-phenyl malonamic acid, when the reaction is performed under high vacuum in dichlorobenzene.

Full text of DOI:10.1002/jhet.5570360439

Products guided by the article

Product name:C₁₅H₂₄N₂O₆Si₂

Cas No:252189-14-3

R&D Labs maybe for 252189-14-3

Tianjin Tensing Fine Chemical Research Develop Centre

Contact:86-022-23718576,13032267585

Address:2-2-201,13 Guiyuan road,Huayuan Industry district,Tianjin,china
Hebei Maison Chemical Co.,Ltd

website:http://www.maisonchem.com.cn

Contact:0086-311-83833777

Address:Leitou industrial district, xinji, shijiazhuang city, hebei province,
Xi'an Galaxy Chemicals CO., Ltd

Contact:86-29-89380370

Address:No.8, Gaoxin three road, Xi'an city.
Taizhou Crene Biotechnology co.ltd

Contact:86-576-88813233 88205808

Address:Economic Developed Zone of Taizhou Zhejiang China
Changzhou Sunlight Pharmaceutical Co., Ltd.

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

Address:JiuliStreet, Benniu Town Changzhou City, Jiangsu Province

Relevant to this article

Formal total synthesis of (-)-anisomycin based on the stereoselective nucleophilic substitution along with aryl migration

Doi:10.1016/S0040-4039(99)01715-3
(1999)
Functional Group Interconversion of Alkylidenemalononitriles to Primary Alcohols by a Cooperative Redox Operation

Doi:10.1055/s-0040-1707184
(2020)
Synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors

Doi:10.1016/S0960-894X(02)00688-1
(2002)
Structural analyses of borane and chloroborane adducts of 1,3,5- dithiaza-, -dioxaza-, -thiadiaza-, and -triazacyclohexanes and their rearrangement products, boracyclohexanes

Doi:10.1002/(sici)1099-0682(199911)1999:11<2063::aid-ejic2063>3.0.co;2-a
(1999)
A convenient synthesis of hindered amines and α-trifluoromethylamines from ketones

Doi:10.1016/S0040-4039(00)97893-6
(1990)
Facile one-pot tandem synthesis of perfluoroalkylated indolizines under metal-free mild conditions

Doi:10.1016/j.tet.2017.01.005
(2017)

Article Doi