A greener enantioselective synthesis of the antiviral agent North-methanocarbathymidine (N-MCT) from 2-deoxy-d-ribose. - Wikidata - wikimedia - TriplyDB

A greener enantioselective synthesis of the antiviral agent North-methanocarbathymidine (N-MCT) from 2-deoxy-d-ribose.

A greener enantioselective synthesis of the antiviral agent North-methanocarbathymidine (N-MCT) from 2-deoxy-d-ribose.

http://www.wikidata.org/entity/Q33978547

about

Advances in the enantioselective synthesis of carbocyclic nucleosides.Efficient synthesis of fluorescent alkynyl C-nucleosides via Sonogashira coupling for the preparation of DNA-based polyfluorophores Highlights in antiviral drug research: antivirals at the horizon.N-O bond as a glycosidic-bond surrogate: synthetic studies toward polyhydroxylated N-alkoxypiperidines.Synthesis of Thienamycin methyl ester from 2-deoxy-D-ribose via Kinugasa reaction.Chemical Synthesis of Carbocyclic Analogues of Nucleosides Recent Advances in the Synthesis of Carbocyclic Nucleosides via Ring-Closing Metathesis

P2860

Q34331725-28E2FAE5-BB8F-4AC5-AEFD-8E48CCAA0D1B Q37072028-F59B18F4-71DD-4C24-8232-C2AB55D8B1F2 Q38007145-0B56EF05-AF0B-4224-9603-85FB42AF9544 Q43494858-398F3398-E314-49E6-A281-4204E3AC7FC8 Q53660304-28C36D2B-C75C-49AF-913E-F8452D9C99B3 Q56864675-234A37A8-A4A6-4FDF-B6CA-D364F6714D73 Q56864676-A9E04304-1800-44E9-8991-295072AEB362

P2860

A greener enantioselective synthesis of the antiviral agent North-methanocarbathymidine (N-MCT) from 2-deoxy-d-ribose.

http://www.wikidata.org/entity/Q33978547

description

2009 nî lūn-bûn

@nan

2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

name

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@ast

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@en

type

label

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@ast

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@en

prefLabel

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@ast

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@en

P1433

Q33978547-F3E7CAA1-3D60-4E5F-AE0C-803B2EE5FA0B

P1476

Q33978547-09144B4F-DDE7-4DA1-BE81-90071901589F

P2093

Q33978547-07FF9744-3045-4D22-9837-5BE450ED1E5D

Q33978547-1D0FC5B2-BBCA-4E43-8882-A6EC0AC57C68

P2860

Q33978547-063E5FB7-ABCE-40D3-94EA-65E9ACBD60C6

Q33978547-20D83F0E-E601-4FD1-A6C4-E75C0254C853

Q33978547-67CC8E7D-9855-4DBD-8FCA-37DC085B4B34

Q33978547-7173AC94-144A-462B-9DD0-D730D24DADF2

Q33978547-8AF24AAA-5AA0-4D80-BAF5-DA0B203C4B75

Q33978547-96843D0D-6CDE-4A0C-90EF-BAB7B2572547

Q33978547-A631757F-1F1C-407A-98DF-F128DD462319

Q33978547-BCE5B7E3-5640-451E-820B-5EC817849398

Q33978547-BFA3E848-76B3-4C0A-BD7A-45D5FB2FC3A9

Q33978547-F11150D1-C701-4D9A-8E5D-112A01B100A8

P304

Q33978547-2D8AC137-5C7A-42C0-A2A3-044C25B3BDB4

P31

Q33978547-92EB771E-E72B-4A90-84B5-0EB163A5CFEC

P356

Q33978547-943107C3-C671-4276-8EE4-BABDC687A5A7

P433

Q33978547-A16AF033-608B-459C-8B65-7EAA113ED02D

P478

Q33978547-A3B8B9E8-A4D6-42A9-AECC-1EE130BF6C61

P577

Q33978547-2A193277-0610-4F0F-B095-7F35B5F55846

P5875

Q33978547-11D43BE4-910E-4B5B-9F2F-FA05B68D2E45

P698

Q33978547-D01BE7ED-6011-41DE-8244-D3ECF0281DE5

P921

Q33978547-E0441838-E445-4FBF-8DAC-5B8C40E43259

Q33978547-F6901C1C-81FF-42A3-95B8-79E2C7FA478D

P932

Q33978547-6942C358-EC30-4D17-8771-F65A26507B3C

P356

J.TET.2009.08.035

P1433

P1476

A greener enantioselective syn ...... (N-MCT) from 2-deoxy-d-ribose.

@en

P2093

Olaf R Ludek

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

Victor E Marquez

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

P2860

Enantioselective synthesis of bicyclo[3.1.0]hexane carbocyclic nucleosides via a lipase-catalyzed asymmetric acetylation. Characterization of an unusual acetal byproduct

Synthesis and antiviral activity of acyclic nucleosides with a 3(S),5-dihydroxypentyl or 4(R)-methoxy-3(S),5-dihydroxypentyl side chain

Potent antiviral activity of north-methanocarbathymidine against Kaposi's sarcoma-associated herpesvirus.

Activity and mechanism of action of N-methanocarbathymidine against herpesvirus and orthopoxvirus infections.

The history of N-methanocarbathymidine: the investigation of a conformational concept leads to the discovery of a potent and selective nucleoside antiviral agent.

Efficacy of N-methanocarbathymidine in treating mice infected intranasally with the IHD and WR strains of vaccinia virus

Preparative and stereoselective synthesis of the versatile intermediate for carbocyclic nucleosides: effects of the bulky protecting groups to enforce facial selectivity.

Cell line dependency for antiviral activity and in vivo efficacy of N-methanocarbathymidine against orthopoxvirus infections in mice.

Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides?

Metabolic pathways of N-methanocarbathymidine, a novel antiviral agent, in native and herpes simplex virus type 1 infected Vero cells.

P304

8461-8467

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

P31

scholarly article

P356

10.1016/J.TET.2009.08.035

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

P433

41

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

P478

65

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

P577

2009-10-01T00:00:00Z

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

P5875

45167908

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

P698

20625519

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

P921

enantioselectivity

(north)-methanocarbathymidine

P932

2900805

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