Orderly Functional Group Dyads. Recognition of Biotin and Adenine Derivatives by a New Synthetic Host

DOI: 10.1021/ja00202a078

Source and publish data:

Journal of the American Chemical Society p. 8055 - 8057 (1989)

Update date:2022-08-04

Topics:

Authors:

Adrian, James C.

Wilcox, Craig S.

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

Article abstract of DOI:10.1021/ja00202a078

Full text of DOI:10.1021/ja00202a078

Products guided by the article

Product name:C₃₁H₂₂N₂O₈

Cas No:123002-54-0

R&D Labs maybe for 123002-54-0

Xiamen Hisunny Chemical Co.,Ltd

website:http://www.hisunnychem.com

Contact:+86-592-3327115

Address:Unit 603,No.879,Xiahe Road,Meixin Building,Xiamen,China
Taimai Sanluck Pharmaceutical Co.,Ltd

Contact:86-592-7662921

Address:8D,No.186,Huarong Road,Huli,Xiamen,China
TIANJIN NORTH JINHENG CHEMICAL PLANT.

Contact:0086-22-59952083

Address:DongShigu Country In JiXian TianJin China
Nanjing Raise Pharmatech Co., Ltd

website:http://www.raisechem.com

Contact:+86-25-58649566

Address:B381,No.606,Ningliu Road,Jiangbei New Area,Nanjing,Jiangsu Province,China
Jiande City Silibase Silicone New Material Manufacture Co., Ltd.

Contact:15967177856

Address:Genglou Industrial Development Area

Relevant to this article

A general and efficient method for the synthesis of silyl-protected arenethiols from aryl halides or triflates

Doi:10.1002/adsc.200404299
(2005)
Phytochemical and Analytical Characterization of Novel Sulfated Coumarins in the Marine Green Macroalga Dasycladus vermicularis (Scopoli) Krasser

Doi:10.3390/molecules23112735
(2018)
Selective Reduction of Pyridazin-3-ones and Ring Contraction to Pyrrolidin-2-ones and 3-Pyrrolin-2-ones

Doi:10.1039/c39840001373
(1984)
Electrochemistry, spectroelectrochemistry, chloride binding, and O ₂ catalytic reactions of free-base porphyrin - Cobalt corrole dyads

Doi:10.1021/ic050738n
(2005)
Insights into the Mechanism of Action of the Two-Peptide Lantibiotic Lacticin 3147

Doi:10.1021/jacs.7b04728
(2017)
Improving the Selectivity of PACE4 Inhibitors through Modifications of the P1 Residue

Doi:10.1021/acs.jmedchem.8b01381
(2018)

Article Doi