A two-step chemical/chiroptical method for determining absolute configurations of α-hydroxy acids

DOI: 10.1016/S0040-4020(98)00221-X

Source and publish data:

Tetrahedron p. 5041 - 5064 (1998)

Update date:2022-08-04

Topics:

Authors:

Rickman, Barry H.

Matile, Stefan

Nakanishi, Koji

Berova, Nina

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

Article abstract of DOI:10.1016/S0040-4020(98)00221-X

A general, chemical/chiroptical approach based on the CD exciton chirality method has been developed to determine the absolute configuration of α-hydroxy acids. This approach consists of amidation of the carboxyl group with ethanolamine followed by deriva

Full text of DOI:10.1016/S0040-4020(98)00221-X

Products guided by the article

Product name:(2S)-N-(2-hydroxyethyl)-2-hydroxy-2-cyclohexylacetamide

Cas No:208462-09-3

R&D Labs maybe for 208462-09-3

Guangzhou Probig Fine Chemical Co., Ltd.

Contact:020-86297874

Address:No.2, 1/F, No.20, Hetai Road,Hebian Village, Baiyun District,Guangzhou,China
Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.
Dalian Synco Chemical Co., Ltd.

Contact:+86-411-83635150

Address:Rm 1004, 24, Tangshan Street, Dalian
NEM CHEMICAL CO.，LTD

website:http://www.NEM.COM.CN

Contact:+86-393-4411771

Address:The west section of shengli Road,Puyang,Henan Province,China
Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK

Relevant to this article

Comparison of phosphonate transition state analogs for inducing catalytic antibodies and evaluation of key structural factors by an ab initio study

Doi:10.1016/S0040-4020(99)00054-X
(1999)
Synthesis and spectral studies on Ru₃(CO)_12-n (μ-Ph₂AsCH₂AsPh₂)(L) (n = 3, L: PPh₃, PCy₂Ph,P(OCH₃)₃); n = 4, L = Ph₂PCH₂PPh₂: Crystal and molecular structures of Ru₃(CO)₉ (μ-Ph₂AsCH₂AsPh₂)(PCy₂Ph)

Doi:10.1016/s0277-5387(97)00406-3
(1998)
Reaction of 1,8-diaminonaphthalene with some selected π-acceptors; Prospective optically active non-linear cyanovinylated naphthalenes as well as synthesis of novel perimidin and pleiadene derivatives

Doi:10.1016/j.tet.2004.03.017
(2004)
Electroactive metallomacromolecules via tetrabis(2,2′:6′,2″-terpyridine)ruthenium(II) complexes: Dendritic nanonetworks toward constitutional isomers and neutral species without external counterions

Doi:10.1021/ja001401h
(2000)
Stereoselective transformation of amines via chiral 2,4,6-triphenylpyridinium intermediates

Doi:10.1016/S0957-4166(01)00343-3
(2001)
A mild method for the synthesis of bis-pyrazolo[3,4-b:4′,3′-e]pyridine derivatives

Doi:10.1016/j.tetlet.2018.09.033
(2018)

Article Doi