CHIROPTICAL PROPERTIES OF TETRAHYDROPYRAN-3,4-DIOLS AND 2-HYDROXYMETHYLTETRAHYDROPYRAN-3-OLS DERIVED FROM L-ARABINOSE, D-GALACTOSE, D-GLUCOSE, AND D-XYLOSE, AND ENANTIOSELECTIVITY IN REDUCTION WITH THEIR COMPLEXES

DOI: 10.1016/0008-6215(88)84002-3

Source and publish data:

Carbohydrate Research p. 179 - 196 (1988)

Update date:2022-08-03

Topics:

Authors:

Snatzke, Guenther

Raza, Zlata

Habus, Ivan

Sunjic, Vitomir

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

Article abstract of DOI:10.1016/0008-6215(88)84002-3

(3R,4R)- (1a) and (3S,4R)-tetrahydropyran-3,4-diol (2a), and (2R,3S)- (3a) and (2R,3R)-2-hydroxymethyltetrahydropyran-3-ol (4a), derived from D-xylose, L-arabinose, D-glucose, and D-galactose, respectively, are structurally the simplest chiral carbohydrat

Full text of DOI:10.1016/0008-6215(88)84002-3

Products guided by the article

Product name:C₂₉H₂₈O₃P₂

Cas No:120019-32-1

R&D Labs maybe for 120019-32-1

Shanghai shibo Chemical Co., Ltd

Contact:+86-021-60753516

Address:688 Qiushi Road, Jinshan High-tech Park, Shanghai, China,201512
Jinan Jianfeng Chemical Co., Ltd

Contact:0086-531-88110457

Address:sales01(-a-t-)pharmachemm{dot}c+o+m
Dragon Chemical Co., Ltd.

Contact:0571-

Address:zhejing
Suzhou Health Chemicals Co., Ltd.

website:http://www.healthchems.com

Contact:13776257979

Address:No. 338, Jingang Avenue,
Tradlon Chemical Co., Ltd.

Contact:+86-710-3516804

Address:Number 83,Panggong road,Xiangcheng District,Xiangyang ,Hubei

Relevant to this article

Nucleosides part LXVI I^[1]: Synthesis of 4-amino-7(8H) pteridinone-N₈-nucleosides-structural analogs of adenosine

Doi:10.1080/15257770903054241
(2009)
[4+2]cycloaddition reactions involving 2-arylmethylidene-1-thiooxoindan intermediates and antimicrobial activity evaluation of some products

Doi:10.1080/10426500701839882
(2009)
Doi:10.1021/jo01095a636
(1958)
Synthesis of P-Chiral Dihydrobenzooxaphosphole Core for BI Ligands in Asymmetric Transformations

Doi:10.1021/acs.joc.7b00491
(2017)
Curcumin analog cytotoxicity against breast cancer cells: exploitation of a redox-dependent mechanism

Doi:10.1016/j.bmcl.2009.10.023
(2009)
Synthesis and SAR study of a novel series of dopamine receptor agonists

Doi:10.1016/j.bmc.2013.11.012
(2014)

Article Doi