Regioselective monodeprotection of peracetylated carbohydrates. - Test2 - elhamkhani - TriplyDB

Regioselective monodeprotection of peracetylated carbohydrates.

Regioselective monodeprotection of peracetylated carbohydrates.

http://www.wikidata.org/entity/Q34407494

about

Regioselective deprotection of the monosaccharide-bearing thiocyanomethyl group at the anomeric position monitored by reversed-phase HPLC method.One-pot synthesis of D-glucosamine and chitobiosyl building blocks catalyzed by triflic acid on molecular sieves.Synthesis of orthogonally protected bacterial, rare-sugar and D-glycosamine building blocks.Synthesis of a heterogeneous artificial metallolipase with chimeric catalytic activity.Regioselective Deacetylation of Disaccharides via ImmobilizedAspergillus nigerEsterase(s)-catalyzed Hydrolysis in Aqueous and Non-aqueous Media Chemoenzymatic synthesis of neoglycoproteins driven by the assessment of protein surface reactivity Regioselective Palmitoylation of 9-(2,3-Dihydroxy- propyl)adenine Catalyzed by a Glycopolymer-enzyme Conjugate

P2860

Q35920117-1EEAEA0D-4A53-4526-B33C-FCEA952C0CB5 Q40155767-58B485F0-8905-44E3-833F-4E1B1FC0057B Q45195236-33FF8DD4-87D8-4C36-A612-D82889E10EE7 Q50978858-2A9D8B3E-4029-401C-8863-8C76EC8453AB Q56036119-4F9F721E-BA9E-41F8-8CB9-2335193BAA44 Q56036811-437F80FF-3601-4CE4-9BB4-6958BC2565EC Q56380762-53C2BBDD-AC86-4C14-BBBE-639A66BB92B4

P2860

Regioselective monodeprotection of peracetylated carbohydrates.

http://www.wikidata.org/entity/Q34407494

description

2012 nî lūn-bûn

@nan

2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Regioselective monodeprotection of peracetylated carbohydrates.

@ast

Regioselective monodeprotection of peracetylated carbohydrates.

@en

Regioselective monodeprotection of peracetylated carbohydrates.

@nl

type

label

Regioselective monodeprotection of peracetylated carbohydrates.

@ast

Regioselective monodeprotection of peracetylated carbohydrates.

@en

Regioselective monodeprotection of peracetylated carbohydrates.

@nl

prefLabel

Regioselective monodeprotection of peracetylated carbohydrates.

@ast

Regioselective monodeprotection of peracetylated carbohydrates.

@en

Regioselective monodeprotection of peracetylated carbohydrates.

@nl

P1433

Q34407494-C11460CD-B3B0-4063-A8CE-79F86E9C552F

P1476

Q34407494-C24261D7-F164-4226-A472-52BCAEFCE3CE

P2093

Q34407494-160463D3-EE65-4F2B-8E6C-DADA54121B96

Q34407494-42CC5271-FFE1-4AEB-8490-AFC2EB89B11A

Q34407494-B40ED7DB-7C2A-4EFA-9E0F-AB4AF4E5045E

P2860

Q34407494-0BC86577-920C-4FA5-A91C-276FDBBE8AFD

Q34407494-0C67B1DD-6C85-476E-A46B-E60A8E6D5186

Q34407494-15282D6C-E452-47D3-877D-4EFDF24BEBD5

Q34407494-2289CEF2-AD14-417A-AA46-2385A37B2965

Q34407494-29E38D3A-2EC6-4349-8C55-A6B093406326

Q34407494-2AB69D09-C72F-4C13-AEFF-EAF9D8535DBF

Q34407494-353026CC-9E52-4692-8F88-3B42ED5EF77A

Q34407494-4D7F71F0-E1B3-4E9C-947D-7A5C8E8D2825

Q34407494-58DE52B7-090A-4740-972C-DC64259200ED

Q34407494-675E3CE6-6B55-47DF-BECE-A91868787CA6

P2888

Q34407494-5FE9F794-135E-472C-A6BF-54911A49A95E

P304

Q34407494-0A4FDB0C-2C96-400C-963D-188D67979CD0

P31

Q34407494-439630B2-F541-432A-8C4A-DDBD4DCBFE92

P356

Q34407494-2F92640B-A8AF-459E-BD21-0244D9E60995

P433

Q34407494-BB3090F9-5C52-41BB-8135-08ED7DED290D

P478

Q34407494-669C7DA2-1A15-4845-B986-D1E81C4E058D

P50

Q34407494-32CE1BFA-A24D-467C-A90B-8E8193E2ACEC

P577

Q34407494-48A0961D-2AF8-40FD-A948-B4CC17EBE106

P5875

Q34407494-8BE25F1F-E9ED-4CE9-93DE-25409BB8D1A2

P6179

Q34407494-F6A498B5-990D-4CEE-8C60-9120E275B647

P698

Q34407494-2BA61471-0B03-4400-A1E2-CCA21D840A09

P356

P1433

Nature Protocols

P1476

Regioselective monodeprotection of peracetylated carbohydrates

@en

P2093

Jose M Guisan

http://www.w3.org/2001/XMLSchema#string

Jose M Palomo

http://www.w3.org/2001/XMLSchema#string

Marco Terreni

http://www.w3.org/2001/XMLSchema#string

P2860

Large-scale approaches for glycobiology.

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

A serine protease triad forms the catalytic centre of a triacylglycerol lipase

Sweet antibiotics - the role of glycosidic residues in antibiotic and antitumor activity and their randomization.

Gangliosides are functional nerve cell ligands for myelin-associated glycoprotein (MAG), an inhibitor of nerve regeneration

Lipases as practical biocatalysts.

Lipases for biotechnology.

Gaucher disease: complexity in a "simple" disorder.

Functions of cell surface galectin-glycoprotein lattices.

Synthesis and medical applications of oligosaccharides.

P2888

P304

1783-1796

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/NPROT.2012.098

http://www.w3.org/2001/XMLSchema#string

P433

10

http://www.w3.org/2001/XMLSchema#string

P478

7

http://www.w3.org/2001/XMLSchema#string

P50

P577

2012-09-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

230811050

http://www.w3.org/2001/XMLSchema#string

P6179

1044823971

http://www.w3.org/2001/XMLSchema#string

P698

22955694

http://www.w3.org/2001/XMLSchema#string