Synthesis of the Monodeoxy Neoglycolipid Analogues of Globotrioside; Development of Some New Methods in Carbohydrate Chemistry.
(1996)- Abstract
- 1. All monodeoxy TMSEt globotriosides (GbO3) and double-chain bis-sulfone GbO3-lipids were synthesised. The alpha-glycosylation with deoxygenated glycosyl donors (fluoride, ethylthio- and thiopyridin-2-yl-) was investigated in the syntheses of the TMSEt 2"-, 3",- 4"- and 6"-deoxy GbO3, and activation of the thiopyridin-2-yl-glycosides with AgOTf gave the best yield and selectivity. Glycosylation with per-benzylated galactosyl chloride and of 2'-, 3'- and 6-deoxy lactosides, under treatment with AgOTf-collidine gave the trisaccharides (37-93%). Selective removal of the protecting group at 6'-O (-TBDMS or -MBn) of GbO3, followed by iodination and reduction gave the 6'-deoxy trisaccharide. DDQ-oxidative removal and rearrangement of... (More)
- 1. All monodeoxy TMSEt globotriosides (GbO3) and double-chain bis-sulfone GbO3-lipids were synthesised. The alpha-glycosylation with deoxygenated glycosyl donors (fluoride, ethylthio- and thiopyridin-2-yl-) was investigated in the syntheses of the TMSEt 2"-, 3",- 4"- and 6"-deoxy GbO3, and activation of the thiopyridin-2-yl-glycosides with AgOTf gave the best yield and selectivity. Glycosylation with per-benzylated galactosyl chloride and of 2'-, 3'- and 6-deoxy lactosides, under treatment with AgOTf-collidine gave the trisaccharides (37-93%). Selective removal of the protecting group at 6'-O (-TBDMS or -MBn) of GbO3, followed by iodination and reduction gave the 6'-deoxy trisaccharide. DDQ-oxidative removal and rearrangement of p-methoxybenzylidene acetals gave the 2- and 3-deoxy- 4-OH acceptors which were glycosylated with different galabiosyl donors and promoters. Only Ag-silicate was mild enough to activate the glycosyl bromide and prevent anomerisation of the 2-deoxy glucoside to give the trisaccharide in 86% yield. NIS-AgOTf-promoted glycosylation with thiophenyl galabioside gave the 3-deoxy TMSEt trisaccharide (92%). Full deprotection gave all the water soluble monodeoxy TMSEt GbO3. Transformation of protected trisaccharides into trichloroacetimidates, via the corresponding hemiacetals, proceeded in (78-96%) overall yield (except for 2-deoxy). Glycosylation of bis-sulfone lipid alcohol with these trichloroacetimidates, proceeded in 37-79% yield, and removal of protecting groups gave the deoxy neoglycolipids. A new synthetic strategy was used in the preparation of the 2-deoxy glycolipid .
2. A method of DDQ-oxidative opening of p-methoxybenzylidene acetals was investigated. The 6-Br and 6-Cl derivatives were obtained in over 90% yield by treatment with a DDQ-halide source, whereas 4-OH-6-OMBz derivatives were obtained (~80%) by treatment with DDQ-H2O-AcOH.
3. The transformation of p-methoxyphenyl glycosides into glycosyl bromides (82-98%), glycosyl chlorides (81-99%) and phenyl thioglycosides (80-100%) was studied.
4. The migration of benzoate under dibutyltin oxide treatment gave 2-OH tri-O-Bz batha-galactosides. Furthermore, the 3-OH and 3,2'-diol per-benzoylated batha-lactosides were prepared in high yields. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/28326
- author
- Zhang, Zhiyuan
- supervisor
- opponent
-
- Lönn, Hans, Astra Draco AB
- publishing date
- 1996
- type
- Thesis
- publication status
- published
- subject
- keywords
- phenyl thioglycoside, glycosyl chloride, glycosyl bromide, 4-methoxyphenyl glycoside, 4-methoxybenzylidene acetal, 6-chlorodeoxy, 6-bromodeoxy, DDQ, 2-deoxy batha-glycoside, glycosylation, deoxy globotrioside, neoglycolipid, anomeric protection, Organic chemistry, Organisk kemi
- pages
- 82 pages
- publisher
- Organic Chemistry, Lund University
- defense location
- Chemical Center, Lecture hall D
- defense date
- 1996-04-11 10:15:00
- external identifiers
-
- other:ISRN: LUTKDH/(TKOK-1027)/1-82/(1996)
- language
- English
- LU publication?
- no
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)
- id
- f29863b2-78af-422d-a1e5-0c60a2874d41 (old id 28326)
- date added to LUP
- 2016-04-04 11:39:57
- date last changed
- 2018-11-21 21:06:22
@phdthesis{f29863b2-78af-422d-a1e5-0c60a2874d41, abstract = {{1. All monodeoxy TMSEt globotriosides (GbO3) and double-chain bis-sulfone GbO3-lipids were synthesised. The alpha-glycosylation with deoxygenated glycosyl donors (fluoride, ethylthio- and thiopyridin-2-yl-) was investigated in the syntheses of the TMSEt 2"-, 3",- 4"- and 6"-deoxy GbO3, and activation of the thiopyridin-2-yl-glycosides with AgOTf gave the best yield and selectivity. Glycosylation with per-benzylated galactosyl chloride and of 2'-, 3'- and 6-deoxy lactosides, under treatment with AgOTf-collidine gave the trisaccharides (37-93%). Selective removal of the protecting group at 6'-O (-TBDMS or -MBn) of GbO3, followed by iodination and reduction gave the 6'-deoxy trisaccharide. DDQ-oxidative removal and rearrangement of p-methoxybenzylidene acetals gave the 2- and 3-deoxy- 4-OH acceptors which were glycosylated with different galabiosyl donors and promoters. Only Ag-silicate was mild enough to activate the glycosyl bromide and prevent anomerisation of the 2-deoxy glucoside to give the trisaccharide in 86% yield. NIS-AgOTf-promoted glycosylation with thiophenyl galabioside gave the 3-deoxy TMSEt trisaccharide (92%). Full deprotection gave all the water soluble monodeoxy TMSEt GbO3. Transformation of protected trisaccharides into trichloroacetimidates, via the corresponding hemiacetals, proceeded in (78-96%) overall yield (except for 2-deoxy). Glycosylation of bis-sulfone lipid alcohol with these trichloroacetimidates, proceeded in 37-79% yield, and removal of protecting groups gave the deoxy neoglycolipids. A new synthetic strategy was used in the preparation of the 2-deoxy glycolipid .<br/><br> <br/><br> 2. A method of DDQ-oxidative opening of p-methoxybenzylidene acetals was investigated. The 6-Br and 6-Cl derivatives were obtained in over 90% yield by treatment with a DDQ-halide source, whereas 4-OH-6-OMBz derivatives were obtained (~80%) by treatment with DDQ-H2O-AcOH.<br/><br> <br/><br> 3. The transformation of p-methoxyphenyl glycosides into glycosyl bromides (82-98%), glycosyl chlorides (81-99%) and phenyl thioglycosides (80-100%) was studied.<br/><br> <br/><br> 4. The migration of benzoate under dibutyltin oxide treatment gave 2-OH tri-O-Bz batha-galactosides. Furthermore, the 3-OH and 3,2'-diol per-benzoylated batha-lactosides were prepared in high yields.}}, author = {{Zhang, Zhiyuan}}, keywords = {{phenyl thioglycoside; glycosyl chloride; glycosyl bromide; 4-methoxyphenyl glycoside; 4-methoxybenzylidene acetal; 6-chlorodeoxy; 6-bromodeoxy; DDQ; 2-deoxy batha-glycoside; glycosylation; deoxy globotrioside; neoglycolipid; anomeric protection; Organic chemistry; Organisk kemi}}, language = {{eng}}, publisher = {{Organic Chemistry, Lund University}}, title = {{Synthesis of the Monodeoxy Neoglycolipid Analogues of Globotrioside; Development of Some New Methods in Carbohydrate Chemistry.}}, year = {{1996}}, }