Acceleration of Hemiacetal Cleavage through Hydrogen Bonding: A New Synthetic Catalyst with Balanced Conformational Flexibility and Preorganization

DOI: 10.1021/jo00010a002

Source and publish data:

Journal of Organic Chemistry p. 3201 - 3203 (1991)

Update date:2022-08-04

Topics:

Authors:

Gennari, Cesare

Molinari, Francesco

Bartoletti, Marcella

Piarulli, Umberto

Potenza, Donatella

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

Article abstract of DOI:10.1021/jo00010a002

Hemiacetal cleavage catalyst 1 was designed, synthesized, and shown to be effective in promoting glycolaldehyde dimer dissociation and tetramethylglucose mutarotation.

Full text of DOI:10.1021/jo00010a002

Products guided by the article

Product name:2,6-Bis-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-benzoic acid ethyl ester

Cas No:133701-02-7

R&D Labs maybe for 133701-02-7

JIANGXI ZHANGFENG CHEMICAL CO., LTD.

Contact:+86-0799-3413066

Address:Xiyuan village, Xiabu Town, Xiangdong District
Sarchem Laboratories, Inc.

Contact:732.938.2777

Address:5012 Industrial Road Farmingdale, NJ 07727
Tianjin Ingenochem Technology Co.,Ltd

Contact:+86-22-23677060

Address:Hitech Green Industry Park K2-9-602, Nankai district
Beijing Zhongshuo Pharmaceutical T & D Co.,Ltd

Contact:0086-10-64430626

Address:ea No 16, HEPINGLI,DONGCHENG DISTRICT,BEIJING,P.R.CHINA.
MedicalChem(Yancheng)Manuf.Co.,Ltd.

Contact:+86-515-84383366

Address:Touzeng BinHai, YanCheng City, JiangSu Province, China

Relevant to this article

Green synthesis of benzamide-dioxoisoindoline derivatives and assessment of their radical scavenging activity – Experimental and theoretical approach

Doi:10.1016/j.tet.2020.131456
(2020)
CONTRIBUTION FROM THE SCHOOL OF CHEMISTRY AND PHYSICS OF THE PENNSYLVANIA STATE COLLEGE: Sterols. CII. Chlorogenin

Doi:10.1021/ja01866a074
(1940)
Efficient low-cost preparation of trans-cyclooctenes using a simplified flow setup for photoisomerization

Doi:10.1007/s00706-016-1668-z
(2016)
Solvolysis of substituted benzyl azoxyarenesulfonates: Characterisation of the transition state and the selectivity of benzylic intermediates in 50% aqueous 2,2,2-trifluoroethanol

Doi:10.1039/b106887n
(2001)
Synthesis of substituted 2-benzoylaminothiobenzamides and their ring closure to substituted 2-phenylquinazoline-4-thiones

Doi:10.3390/60400323
(2001)
Synthesis of novel cationic lipids: Effect of structural modification on the efficiency of gene transfer

Doi:10.1021/jm010918g
(2002)

Article Doi