Metal substituted diazo esters as substrates for cross coupling reactions

DOI: 10.1016/S0040-4020(96)01194-5

Source and publish data:

Tetrahedron p. 2371 - 2386 (1997)

Update date:2022-07-29

Topics:

Authors:

Padwa, Albert

Sa, Marcus M.

Weingarten, M. David

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

Article abstract of DOI:10.1016/S0040-4020(96)01194-5

Ethyl (trialkylstannyl)diazoacetates have been employed as substrates in the Stille reaction, The palladium(O)-catalyzed cross coupling works well with aryl iodides but not with acyl or aryl chlorides. Bis-[ethoxycarbonyl-diazomethyl]-mercury showed high

Full text of DOI:10.1016/S0040-4020(96)01194-5

Products guided by the article

Product name:ethyl 4,12b-epoxy-3a,4,5,6,12b,12c-hexahydro-1,3,5,8-tetraoxo-1H-pyrrolo<3,4-k>5H-azepino<2,1-a>isoindole-4-carboxylate

Cas No:126686-04-2

R&D Labs maybe for 126686-04-2

KindChem Co.,Ltd,

Contact:+86-25-85281586

Address:13F,Bld2#,South of Longpan Road
Zhejiang Hoshine Silicon Industry Co., Ltd.

Contact:86-573-89179966

Address:Zhapu Town, Pinghu City, Zhejiang, China
Zhangjiagang Jianing Import & Export Co.,Ltd.

Contact:086-512-55379012 13913607595

Address:NO.1 Guotai North Road Zhangjiagang Economic Development Zone,215600,Jiangsu,China
Shandong Xiangde Biotechnology Co., Ltd

Contact:+86 -15066639877

Address:Sanba street
Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone

Relevant to this article

Decarbonylative cycloaddition of phthalic anhydrides with allenes

Doi:10.1021/ol200044y
(2011)
Reaktionen pyrazolatoverbrueckter Dirutheniumcluster mit Diphosphanen. Synthese und Festkoerperstuktur von (μ₂-H)Ru2(CO)3(μ₂-η²-3,5-Me2N2C3H)2-<μ₁-η²-PPh2CH2CH2PPh(C6H4)>

Doi:10.1016/0022-328X(89)80034-8
(1989)
Pd(ii)-catalyzed decarboxylative allylation and Heck-coupling of arene carboxylates with allylic halides and esters

Doi:10.1039/c0ob00696c
(2011)
Selective Inhibitors of G2019S-LRRK2 Kinase Activity

Doi:10.1021/acs.jmedchem.0c01243
(2020)
1,2-Addition of Sulfur Nucleophiles to the N-Acylated Imine Linkage. A Model Study for the Incorporation of Sulfur Nucleophiles during Metabolism of Acylated Aromatic Amines

Doi:10.1021/jo00300a002
(1990)
Discovery of 4-alkoxy-2-aryl-6,7-dimethoxyquinolines as a new class of topoisomerase I inhibitors endowed with potent in vitro anticancer activity

Doi:10.1016/j.ejmech.2021.113261
(2021)

Article Doi