SELECTIVE REDUCTION OF AROMATIC / ALIPHATIC NITRO GROUPS BY SODIUM SULFIDE.

DOI: 10.1016/S0040-4039(00)80169-0

Source and publish data:

Tetrahedron Letters p. 635 - 638 (1988)

Update date:2022-08-05

Topics:

Authors:

Huber, Didier

Andermann, Guy

Lecrerc, Gerard

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

Article abstract of DOI:10.1016/S0040-4039(00)80169-0

Sodium sulfide can be used to reduce selectively aromatic / aliphatic nitro groups.In the absence of water, the aromatic nitro group can be reduced selectively in the presence of a secondary aliphatic one.However, in the presence of a tertiary aliphatic n

Full text of DOI:10.1016/S0040-4039(00)80169-0

Products guided by the article

Product name:4-(2-Methyl-propenyl)-phenylamine

Cas No:116760-99-7

R&D Labs maybe for 116760-99-7

LIAOYANG WANRONG CHEMICALS COMPANY LIMITED

Contact:86-419-2390789

Address:XINLI VILLAGE , DONG NINGWEI COUNTY,TAIZIHE DISTRICT, LIAOYANG , LIAONING
Chongqing KonAo Health Co.,Ltd

Contact:13687578375

Address:wuhan hubei china
Shanghai Kangxin Chemical Co., Ltd

Contact:+86 21 60717227

Address:118,Ganbai Village,Waigang Town,Jiading District,Shanghai
Fujian Wanke Pharmaceutical Co., LTD.

Contact:+86-598-5026002

Address:Economic development zone,jiangle county
Changzhou Sunsheng Chem Co., Ltd

Contact:+1-(989)-854-0648

Address:No. 28 Yinshan Rd., Xixiashu Industrial Park

Relevant to this article

Doi:10.1021/jo01094a628
(1959)
Total synthesis of graphislactones A, C, D, and H, of ulocladol, and of the originally proposed and revised structures of graphislactones e and F

Doi:10.1002/ejoc.200801278
(2009)
Synthesis of (-)-Oxetanocin

Doi:10.1021/ja00229a048
(1988)
Highly stereoselective and efficient synthesis of ω-heterofunctional di- and trienoic esters for Horner-Wadsworth-Emmons reaction via alkyne hydrozirconation and Pd-catalyzed alkenylation

Doi:10.1016/j.tetlet.2009.02.023
(2009)
IBX/TBAB-mediated oxidation of primary amines to nitriles

Doi:10.1055/s-0028-1087994
(2009)
Synthetic studies of (±)-lysergic acid and related compounds

Doi:10.1248/cpb.35.4793
(1987)

Article Doi