SYNTHESIS OF METHYL 2,3-O-D-GLYCOPYRANOSYLIDENE α-D-MANNOPYRANOSIDES HAVING VARIOUS SUBSTITUENTS

DOI: 10.1016/0008-6215(83)84016-6

Source and publish data:

Carbohydrate Research p. 187 - 204 (1983)

Update date:2022-08-04

Topics:

Authors:

Yoshimura, Juji

Asano, Katsuji

Umemura, Kazuyuki

Horito, Shigeomi

Hashimoto, Hironobu

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

Article abstract of DOI:10.1016/0008-6215(83)84016-6

The title compounds were obtained by condensation of D-glucono-, D-galactono-, or L-glycero-D-gluco-heptono-1,5-lactones with methyl 2,3-di-O-(trimethylsilyl)-α-D-mannopyranosides having various substituents on C-4 and C-6, in the presence of trimethylsil

Full text of DOI:10.1016/0008-6215(83)84016-6

Products guided by the article

Product name:methyl 4,6-di-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-α-D-mannopyranoside

Cas No:88713-96-6

R&D Labs maybe for 88713-96-6

Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,China
shijiazhuang shuanglian chemical industry co.,ltd

Contact:0311-82190302

Address:Luquan Intersection , Shijiazhuang--Taiyuan Expressway，Shijiazhuang City
Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
Nanjing Duly Biotech Co., Ltd

website:http://www.dulynet.com/

Contact:025-84699383 -8003

Address:Room 503, Building 2, Chuangxinhui, No. 61 Wenjing Road, High-tech Development Zone, Pukou District, Nanjing City, Jiangsu Province Nanjing, Jiangsu
Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072

Relevant to this article

4,6-O-[1-cyano-2-(2-iodophenyl)ethylidene] acetals. Improved second-generation acetals for the stereoselective formation of β-D-mannopyranosides and regioselective reductive radical fragmentation to β-D-rhamnopyranosides. Scope and limitations

Doi:10.1021/jo0526688
(2006)
Modified coumarins. 29. Synthesis of structural analogs of natural 6-arylfuro[3,2-g]chromen-7-ones

Doi:10.1007/s10600-009-9261-x
(2009)
Nitrone Formation by Reaction of an Enolate with a Nitro Group

Doi:10.1021/acs.orglett.1c00603
(2021)
PHOTOCHEMICAL OXIDATION AND DIMERIZATION OF ALKYLBENZENES. SELECTIVE REACTIONS OF THE ALKYL SIDE GROUPS

Doi:10.1016/S0040-4039(00)88319-7
(1983)
Indazole N-oxide derivatives as antiprotozoal agents: Synthesis, biological evaluation and mechanism of action studies

Doi:10.1016/j.bmc.2006.01.007
(2006)
Synthesis of archaeal bipolar lipid analogues: A way to versatile drug/gene delivery systems

Doi:10.1021/jo071181r
(2007)

Article Doi