SYNTHESIS AND GLYCOSIDATION REACTIONS OF ACETYLATED RACEMIC PSEUDOGLYCALS

DOI: 10.1016/S0008-6215(00)85244-1

Source and publish data:

Carbohydrate Research p. 193 - 202 (1981)

Update date:2022-09-26

Topics:

Authors:

Angerbauer, Rolf

Schmidt, Richard R.

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

Article abstract of DOI:10.1016/S0008-6215(00)85244-1

The Diels-Alder reaction of 1,3-butadienylene diacetate with activated carbonyl compounds yields O-acetylated pseudoglycals (hex-2-enopyranoses).These reactive compounds are used for highly stereoselective syntheses of α-glycosides.Conformational analysis

Full text of DOI:10.1016/S0008-6215(00)85244-1

Products guided by the article

Product name:3-Acetoxy-6-((3aR,4R,6R,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethoxy)-3,6-dihydro-2H-pyran-2-carboxylic acid butyl ester

Cas No:64035-93-4

R&D Labs maybe for 64035-93-4

Huludao Tianqi Shengye Chemical Co.,Ltd.

Contact:0086 429 2075777

Address:Area B,Shipbuilding Industry Park,Beigang District,Huludao City,Liaoning prov.,China
Laohekou Jinghong Chemical Co.,Ltd

Contact:+86-0710-3702747

Address:163.East，Huagong Road，Laohekou
Jiangxi Hessence Chemicals Co., Ltd.

Contact:+86 796 3511924

Address:Chengxi Industrial Park, Jishui County, Jiangxi Province 331600 China.
KINHENG CHEMICAL(SHANGHAI)CO., LTD.

Contact:+8621-60490170

Address:Room401, No.28,Lane 189, Yangshupu Rd. Shanghai, China.
ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.

website:http://www.zenvasino.com

Contact:+86-138-72658998

Address:Shibeishan Road,Zhijiang, Hubei, China

Relevant to this article

Doi:10.1021/ja01848a005
(1941)
Convenient and efficient synthesis of 1,1-bis-(4-alkylthiophenyl)-1-alkenes via tandem Friedel-Crafts acylation and alkylation of sulfides and acyl chlorides

Doi:10.1080/00397910500187373
(2005)
Synthesis of N-functionalized carbodiimides, hydantoins, 1,3-diazetidines, and imidazolidine derivatives from N-vinylic phosphazenes derived from β-amino acids

Doi:10.3987/COM-01-9264
(2001)
Carbocyclic Substrate Analogues Reveal Kanosamine Biosynthesis Begins with the α-Anomer of Glucose 6-Phosphate

Doi:10.1021/acschembio.0c00409
(2020)
A SIMPLE SYNTHESIS OF α,β-UNSATURATED CARBONYL COMPOUNDS BY TRAPPING THE MICHAEL ADDITION-ENOLATE ANION WITH METHANESULFINYL CHLORIDE

Doi:10.1246/cl.1981.1159
(1981)
Microbiological Reduction of α,β-Unsaturated Ketones by Beauveria sulfurescens

Doi:10.1021/jo00344a009
(1982)

Article Doi