Reductive decarboxylation of N-(acyloxy)phthalimides via redox-initiated radical chain mechanism

DOI: 10.1016/S0040-4039(00)60192-2

Source and publish data:

Tetrahedron Letters p. 7377 - 7380 (1992)

Update date:2022-08-17

Topics:

Authors:

Okada Okada

Okubo Okubo

Morita Morita

Oda Oda

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

Article abstract of DOI:10.1016/S0040-4039(00)60192-2

Highly efficient reductive decarboxylation of N-(acyloxy)phthalimides which are readily prepared from carboxylic acids was achieved by visible light irradiation using Ru(bpy)₃Cl₂ as a sensitizer in the presence of BNAH and t-BuSH via radical chain mechanism.

Full text of DOI:10.1016/S0040-4039(00)60192-2

Products guided by the article

Product name:1,3-DIPHENYLPROPANE

Cas No:1081-75-0

R&D Labs maybe for 1081-75-0

Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,China
Shanghai chemrole co.,ltd

Contact:021-50278900

Address:No.6,Room 201 ,Lane 299,bisheng road ,shanghai ,china
Nanjing Fubang Chemical Co.,Ltd

Contact:+86-25-83179199

Address:5F,Tianzheng international plaza,No399 Zhongyang Road ,Nanjing China
Weihao Chemtech (ChangZhou) Co., Ltd.(expird)

Contact:051989185693

Address:NO 217 huangshan Rd ,Changzhou

Relevant to this article

Doi:10.1021/jo01038a522
(1963)
Newly synthesized oleylgingerol and oleylshogaol activate TRPV1 ion channels

Doi:10.1271/bbb.70187
(2007)
Siloxanes with pendent naphthalene diimides: Synthesis and fluorescence quenching

Doi:10.1021/ol070562o
(2007)
One-pot green and efficient synthesis of xanthenedione derivatives using [C₄ (mim) ₂](FeCl₄)₂ as a magnetic room temperature dicationic ionic liquid

Doi:10.13005/ojc/310158
(2015)
Reactions of vanadium(IV) and (V) with s² metal-ion reducing centers

Doi:10.1039/b306566a
(2003)
A new organic far-red mechanofluorochromic compound derived from cyano-substituted diarylethene

Doi:10.1016/j.tet.2013.10.066
(2013)

Article Doi