Reactivity of glycopyranosyl trichloroacetimidates with air-oxidised samarium diiodide in tetrahydrofuran

DOI: 10.1016/S0040-4039(98)01052-1

Source and publish data:

Tetrahedron Letters p. 5605 - 5608 (1998)

Update date:2022-08-02

Topics:

Authors:

Adinolfi, Matteo

Barone, Gaspare

Iadonisi, Alfonso

Lanzetta, Rosa

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

Article abstract of DOI:10.1016/S0040-4039(98)01052-1

Glycopyranosyl trichloroacetimidates react with SmI₂/O₂/THF to give 4- iodo-n-butyl 1,2-transglycopyranosides. Good to high yields can be obtained from 2α-O-acylated trichloroacetimidates. With armed or manno substrates competitive f

Full text of DOI:10.1016/S0040-4039(98)01052-1

Products guided by the article

Product name:2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl iodide

Cas No:53008-62-1

R&D Labs maybe for 53008-62-1

EGBERT CORPORATION

Contact:+86 18616952870

Address:Area
Hangzhou Pharma & Chem Co.,Ltd.

Contact:+86-571-87040515

Address:No,139Qingchun Rd
Zhejiang Kangfeng Chemical Co.,LTD.

Contact:+86-579-86709687

Address:Xueshizhai Industrial Zone, Weishan Town,Dongyang City, Zhejiang Province ,China
TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
Shijiazhuang Sdyano Fine Chemical Co., Ltd

Contact:+86-311-89830448

Address:NO.48 Ta Nan Road,Yuhua District,Shijiazhuang,Hebei,China

Relevant to this article

ASYMMETRIC ALDOL REACTION OF AN ISOCYANOACETATE WITH ALDEHYDES CATALYZED BY CHIRAL FERROCENYLPHOSPHINE-GOLD(I) COMPLEXES: DESIGN AND PREPARATION OF NEW EFFICIENT FERROCENYLPHOSPHINE LIGANDS

Doi:10.1016/S0040-4039(00)61850-6
(1987)
SKATTEBOL TYPE REARRANGEMENT VIA α-BROMOTRIMETHYLSTANNYL CYCLOPROPANE THERMOLYSIS. WHAT IS THE MECHANISM?

Doi:10.1016/S0040-4039(01)91253-5
(1984)
Synthesis, XRD, EXAFS and XANES study of Cu(II) complexes of aniline dithiocarbamate

Doi:10.14233/ajchem.2020.22456
(2020)
The Application of 2-Benzyl-1,4-naphthoquinones as Pronucleophiles in Aminocatalytic Synthesis of Tricyclic Derivatives

Doi:10.1021/acs.joc.8b00170
(2018)
Doi:10.1002/9780470132364.ch13
(1957)
Doi:10.1021/ja01611a059
(1955)

Article Doi