The effect of neighbouring group participation and possible long range remote group participation in O-glycosylation

• Rituparna Das and
• Balaram Mukhopadhyay

Beilstein J. Org. Chem. 2025, 21, 369–406, doi:10.3762/bjoc.21.27

• stereoselective glycosylation reactions with 2,4,6-trimethoxythiophenyl protection and 2,4-dichlorobenzyl-protection in the O-2 position [152]. In sync with the protocol of chiral stereodirecting protecting groups by Boons, Fairbanks and co-workers also implemented the trimethoxy-substituted thiophenonium group

A study of the DIBAL-promoted selective debenzylation of α-cyclodextrin protected with two different benzyl groups

• Naser-Abdul Yousefi,
• Morten L. Zimmermann and
• Mikael Bols

Beilstein J. Org. Chem. 2022, 18, 1553–1559, doi:10.3762/bjoc.18.165

• Naser-Abdul Yousefi Morten L. Zimmermann Mikael Bols Department of chemistry, University of Copenhagen, Universitetsparken 5, 2100, Copenhagen, Denmark 10.3762/bjoc.18.165 Abstract An α-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the

• ; cyclodextrin; debenzylation; 2,4-dichlorobenzyl; selective; Introduction α-Cyclodextrin (1) is a cyclic carbohydrate consisting of six α-1,4-linked ᴅ-glucose molecules (Figure 1). It has a donut-like structure with the glucose residues all aligned with the α-side towards the center of the ring and the polar

• electron-poor benzyl groups reacting much more sluggishly. Indeed the per-2,4-dichlorobenzyl (DCB) protected compound 1 was completely resistant to DIBAL even when treated for several days [15]. This led us to wonder if an α-cyclodextrin protected on the primary hydroxy groups with DCB groups and on the

Concise total synthesis of two marine natural nucleosides: trachycladines A and B

• Haixin Ding,
• Wei Li,
• Zhizhong Ruan,
• Ruchun Yang,
• Zhijie Mao,
• Qiang Xiao and
• Jun Wu

Beilstein J. Org. Chem. 2014, 10, 1681–1685, doi:10.3762/bjoc.10.176

• a mixture of anomers (α:β = 2:3, 93% for two steps). Then, the other two hydroxy groups were protected as 2,4-dichlorobenzyl ether. Compound 8 was isolated in 95% yield after reacting compound 7 with NaH and 2,4-dichlorobenzyl chloride in anhydrous DMF. 2,4-Dichlorobenzyl chloride was used because

• it is less irritant than the usually used benzyl bromide. Regioselective cleavage of the 2-O-(2,4-dichlorobenzyl) group was attempted with anhydrous SnCl4 in DCM by the method reported by Brown [31][32] and our group [16]. To our delight, this approach can afford 3-O-(2,4-dichlorobenzyl)-1-O-methyl-α

• correlations of H-1, H-3, 5-CH3 and 2-β-methyl. Then, the remaining 3-(O-2,4-dichlorobenzyl) group was removed under hydrogenation with 20% Pd(OH)2/C as a catalyst to give 12 in 91% yield. As the anomerization of the 1-O-α-methyl glycoside may occur under acidic conditions, the structural characterization may