NOVEL CYCLODEXTRIN-OLIGOSILOXANE COPOLYMERS AND THEIR USE AS STATIONARY PHASES FOR SEPARATING ENANTIOMERS IN OPEN TUBULAR COLUMN SUPERCRITICAL FLUID CHROMATOGRAPHY

DOI: 10.1016/S0040-4039(00)60062-X

Source and publish data:

Tetrahedron Letters p. 79 - 82 (1993)

Update date:2022-08-04

Topics:

Authors:

Bradshaw, Jerald S.

Yi, Guoliang

Rossiter, Bryant E.

Reese, Shawn L.

Petersson, Patrik

et al. et al.

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

Article abstract of DOI:10.1016/S0040-4039(00)60062-X

New stationary phases composed of cyclodextrin-oligosiloxane copolymers for open tubular column supercritical fluid chromatography have been developed.These phases allow the separation of enantiomers of a variety of chiral organic solutes.

Full text of DOI:10.1016/S0040-4039(00)60062-X

Products guided by the article

Product name:6^A,6^B-bis-O-heptakis(2,3-di-O-methyl)-β-cyclodextrin

Cas No:146099-67-4

R&D Labs maybe for 146099-67-4

LIAONING DMSO CHEMICALS CO.,LTD.

website:http://www.chinadmso.com

Contact:+86-427-6503033

Address:FLOOR 16, BLOCK A, FINANCIAL SQUARE, XINGLONGTAI DISTRICT, PANJIN CITY, LIAONING P.R. CHINA
Hubei Onward Bio-Development Co., Ltd.

Contact:+86-718-8417012

Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
Molobelamltrading

Contact:27-792-602929

Address:SIDNEY MUFAMADI STREET 009949 X44 0700 POLOKWANE,LIMPOPO
Shandong Hongxiang Zinc Co., Ltd

Contact:086-0311-66187879

Address:DaWang developing zone

Relevant to this article

Synthesis, antitubercular and anticancer activity of new Baylis-Hillman adduct-derived N-cinnamyl-substituted isatin derivatives

Doi:10.1007/s00044-013-0787-x
(2014)
Selective synthesis of optically active 3-haloazetidin-2-ones or aziridines by the condensation of various metal enolates of α-haloacetate with a chiral imine

Doi:10.1016/S0040-4039(00)74774-5
(1992)
Synthesis of enantiomerically pure β- and γ-amino acids from aspartic and glutamic acid derivatives

Doi:10.1055/s-1992-26315
(1992)
A highly efficient method for the preparation of phosphinic pseudodipeptidic blocks suitably protected for solid-phase peptide synthesis

Doi:10.1016/S0040-4020(01)00221-6
(2001)
Visible-Light-Mediated S?H Bond Insertion Reactions of Diazoalkanes with Cysteine Residues in Batch and Flow

Doi:10.1002/adsc.202000716
(2020)
First total synthesis of scopadulcic acid B

Doi:10.1021/ja00058a064
(1993)

Article Doi