Synthesis and selective molecular recognition of a macroatricyclic receptor having crown ether and cyclophane subunits as binding sites

DOI: 10.1021/ja00159a039

Source and publish data:

Journal of the American Chemical Society p. 1144 - 1150 (1990)

Update date:2022-07-30

Topics:

Authors:

Saigo Saigo

Kihara Kihara

Hashimoto

Lin Lin

Fujimura

Suz uki Suz uki

Hasegawa

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

Article abstract of DOI:10.1021/ja00159a039

The synthesis and selective molecular recognition of a new type of cylindrical, macrotricyclic receptor (1) having crown ether and cyclophane subunits as binding sites and a large hydrophobic cavity are described. Receptor 1 was synthesized by the stepwis

Full text of DOI:10.1021/ja00159a039

Products guided by the article

Product name:C₁₀₈H₁₀₀N₄O₁₆S₂

Cas No:106527-61-1

R&D Labs maybe for 106527-61-1

TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
Hongyi Import & Export CO.,LTD

Contact:86-13319649499

Address:Nanzheng Neighborhood Commitees, Chongwen Office, Yongding District
Taixing Shenfeng Chemical Co., Ltd.

Contact:+86-523-87117033, 87117666

Address:4# Yinsanlu, Huangqiao town, Taixing, Jiangsu, China.
Hangzhou GreenCo Science & Technology Co., Ltd.

Contact:86-571-88257303

Address:1713 Room,Jingui Building,Gudun Road,Xihu District,Hangzhou,China
Shanghai Send Pharmaceutical Technology Co., Ltd.

website:http://www.shsendpharma.com

Contact:021-58088081, +8613585868794

Address::Room A601, Building 1,NO. 800 Qingdai Road Pudong District Shanghai,China

Relevant to this article

One-electron-reduced and -oxidized stages of donor-substituted 1,1,4,4-tetracyanobuta-1,3-dienes of different molecular architectures

Doi:10.1002/chem.200800716
(2008)
Ring contraction during the 6π-electrocyclisation of naphthopyran valence tautomers

Doi:10.1039/b807744d
(2008)
Linked macrocyclic systems. Interaction of copper(I) with tris-ring N₂S₂-donor macrocycles and their single-ring analogues

Doi:10.1016/j.inoche.2007.06.002
(2007)
Fourteen-electron organoiron species: Synthesis and characterization of high-spin iron(II) alkyls and the crystal structure of the benzyl derivative Fe(CH₂C₆H₄CH₃)₂(dippe)

Doi:10.1021/om00147a014
(1987)
Ugi four-component reaction with tandem deprotection, cyclization and pictet-spengler reaction: A concise route to N-fused polycyclic indoledi-ketopiperazine alkaloid analogues

Doi:10.1055/s-0033-1338707
(2013)
Carbon-carbon bond formations at the benzylic positions of N-benzylxanthone imines and N-benzyldi-1-naphthyl ketone imine

Doi:10.1016/j.tet.2009.02.034
(2009)

Article Doi