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

Shanghai Korey Pharm Co.,Ltd.(expird)

Contact:021-61840961 021-61840962

Address:No.157,Zhuguang Rd, Qingpu, Shanghai, China
QINGDAO TAOSIGN INTERNATIONAL TRADE CO.,LIMITED

Contact:+86-0532-82683616

Address:RM1402, Doublestar Seacoase 7#, No. 5 Guizhou Road, Qingdao, Shandong, China
Linyi Shengxin Pharmaceutical R&D Co., Ltd

Contact:+86-18653953873

Address:West First of Yufeng Road, Yishui County
Hubei Onward Bio-Development Co., Ltd.

Contact:+86-718-8417012

Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
Nanjing Spring & Autumn Biological Engineering Co., Ltd.

Contact:86-180510-83338

Address:Suite# 210, No. 1 BuildingNanjing Agricultural Biotechnology High-tech Entrepreneurship Center, No. 4 Tongwei Road, Xuanwu District, Nanjing,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