Synthesis of β phenylethylamine derivatives. X. N (hydroxy and methoxy aralkyl) derivatives

DOI: 10.1002/recl.19730921113

Source and publish data:

Recueil des Travaux Chimiques des Pays-Bas p. 1281 - 1297 (1973)

Update date:2022-08-03

Topics:

Authors:

Van Dijk

Moed Moed

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

Article abstract of DOI:10.1002/recl.19730921113

Full text of DOI:10.1002/recl.19730921113

Products guided by the article

Product name:Benzenemethanol, 4-hydroxy-a-[[[2-(4-methoxyphenyl)ethyl]amino]methyl]-, (R)-

Cas No:105199-88-0

R&D Labs maybe for 105199-88-0

Cerametek Materials（ShenZhen）Co., Ltd.

Contact:+86-755-2324.2554

Address:A3-#9, YongChuan Street, Suite 501
WUXI HONOR SHINE CHEMICAL CO.,LTD

Contact:+86-510-83593312

Address:No.1699 Huishan avenue,Huishan district,Wuxi ,Jiangsu,China,214177.(Wuxi Huishan Ecomonic Develop Zone )
Changyi Xinxing Technology Development Co., Ltd.

Contact:0086-510-86651065(Time Zone:8),86651656

Address:94 Yingbinxilu WestRoad, Huangtu Town, Jiangyin City, Jiangsu, China
QINGDAO HONG JIN CHEMICAL CO.,LTD.

website:http://www.hongjinchem.com

Contact:+86-532-83657313

Address:2ND Building, 8 Shangqing Road, Qingdao, Shandong Province, China.
Nantong Kaixin Pharma Chemical Co.,Ltd.

Contact:86-513-85250786

Address:2-1103 Huachen Mansion, 111 Gongnong Road,Nantong, Jiangsu, China

Relevant to this article

Rh-Catalyzed asymmetric hydroaminomethylation of α-Substituted acrylamides: Application in the synthesis of RWAY

Doi:10.1021/acs.orglett.0c03433
(2020)
Synthesis and biological evaluation of sulfur-containing shikonin oxime derivatives as potential antineoplastic agents

Doi:10.1016/j.ejmech.2017.11.031
(2018)
Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones

Doi:10.1039/c3ob41437j
(2013)
Cyclopentadienyl and pentamethylcyclopentadienyl ruthenium complexes as catalysts for the total deoxygenation of 1,2-hexanediol and glycerol

Doi:10.1039/c0gc00255k
(2011)
A photolabile ligand for light-activated release of caged copper

Doi:10.1021/ja8047442
(2008)
Doi:10.1007/BF00905674
(1959)

Article Doi