27086-14-2

Upstream product

• 39686-94-7 1,2,4,6-tetra-O-acetyl-3-O-benzyl-β-D-glucopyranose 

Downstream Products

• 68537-69-9 1,2,4,6-tetra-O-acetyl-3-O-p-tolylsulfonyl-β-D-glucopyranose 
• 140420-82-2 O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-1,2,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 124595-22-8 Acetic acid (2S,3R,4S,5R,6R)-5-acetoxy-6-acetoxymethyl-2-phenylsulfanyl-4-trimethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 124595-22-8 Acetic acid (2R,3R,4S,5R,6R)-5-acetoxy-6-acetoxymethyl-2-phenylsulfanyl-4-trimethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 124595-21-7 Acetic acid (2S,3R,4S,5S,6R)-5-acetoxy-6-acetoxymethyl-4-hydroxy-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester 
• 99337-72-1 1,2,4,6-tetra-O-acetyl-3-O-trityl-β-D-glucopyranose 
• 124608-69-1 Acetic acid (2S,3R,4S,5R,6R)-5-acetoxy-6-acetoxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester 
• 124608-69-1 Acetic acid (2R,3R,4S,5R,6R)-5-acetoxy-6-acetoxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester 
• 140420-87-7 O-(3-O-allyl-2,4,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-1,2,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 140420-86-6 O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-1,2,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 130052-87-8 Acetic acid (2R,3R,4S,5R,6S)-5,6-diacetoxy-2-acetoxymethyl-4-trimethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 22352-62-1 laminaribiose octaacetate 
• 140420-90-2 O-(3-O-allyl-2,4,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-α-D-glucopyranosyl)-1,2,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 140420-91-3 O-(2,4,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-1,2,4,6-tetra-O-acetyl-β-D-glucopyranose 

Relevant academic research and scientific papers

Visible-Light-Mediated Oxidative Debenzylation Enables the Use of Benzyl Ethers as Temporary Protecting Groups

The cleavage of benzyl ethers by catalytic hydrogenolysis or Birch reduction suffers from poor functional group compatibility and limits their use as a protecting group. The visible-light-mediated debenzylation disclosed here renders benzyl ethers temporary protective groups, enabling new orthogonal protection strategies. Using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) as a stoichiometric or catalytic photooxidant, benzyl ethers can be cleaved in the presence of azides, alkenes, and alkynes. The reaction time can be reduced from hours to minutes in continuous flow.