The synthesis of RNA containing the modified nucleotides N2- methylguanosine and N6,N6-dimethyladenosine

DOI: 10.1080/07328319808004317

Source and publish data:

Nucleosides and Nucleotides p. 2281 - 2288 (1998)

Update date:2022-08-03

Topics:

Authors:

Rife, Jason P.

Cheng, Charles S.

Moore, Peter B.

Strobel, Scott A.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1080/07328319808004317

The phosphoramidites of the naturally occurring modified nucleotides N²-methylguanosine and N⁶, N⁶-dimethyladenosine were synthesized and incorporated into short oligoribonucleotides. Described are the syntheses of the phosphoramidites and the procedures used to deprotect oligoribonucleotides in which the O⁶ of m²G is protected with a 2-(p- nitrophenyl)ethyl group.

Full text of DOI:10.1080/07328319808004317

Nucleosides and Nucleotides

ISSN: 0732-8311 (Print) (Online) Journal homepage: http://www.tandfonline.com/loi/lncn19

The Synthesis of RNA Containing the Modified

Nucleotides N ²-Methylguanosine and N ⁶, N ⁶-

Dimethyladenosine

Jason P. Rife , Charles S. Cheng , Peter B. Moore & Scott A. Strobel

To cite this article: Jason P. Rife , Charles S. Cheng , Peter B. Moore & Scott A. Strobel

(1998) The Synthesis of RNA Containing the Modified Nucleotides N ²-Methylguanosine

and N ⁶, N ⁶-Dimethyladenosine, Nucleosides and Nucleotides, 17:12, 2281-2288, DOI:

10.1080/07328319808004317

To link to this article: http://dx.doi.org/10.1080/07328319808004317

Published online: 16 Aug 2006.

Submit your article to this journal

Article views: 28

View related articles

Citing articles: 3 View citing articles

Full Terms & Conditions of access and use can be found at

http://www.tandfonline.com/action/journalInformation?journalCode=lncn19

Download by: [University of Florida]

Date: 16 June 2016, At: 23:12

Products guided by the article

Product name:5'-O-monomethoxytrityl-N₆,N₆-dimethyladenosine

Cas No:57881-34-2

R&D Labs maybe for 57881-34-2

NINGBO PANGS CHEM INT’L CO., LTD.

Contact:+86-0574-27666801

Address:Floor 21, Building 11, Xintiandi, No. 689, Shijiroad, Ningbo, Zhejiang, China
SHANGHAI ARCADIA BIOTECHNOLOGY LTD.

Contact:+86-21-61353236

Address:SUITE 901, BUILDING WENSLI, 1378 LU JIA BANG RD, SHANGAHI 200011, P.R.CHINA
Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.
Xi'an North Information Industry Co., Ltd. Weilv Chemical Department

Contact:+86-29-88156413

Address:Jixiang Road 99 Xi'an Shaanxi Province
SuZhou LaiTeou

Contact:+86-0512-88957371

Address:shanghai

Relevant to this article

Enantiospecific first total synthesis and assignment of absolute configuration of the sesquiterpene (-)-cucumin H

Doi:10.1021/ol034635p
(2003)
Doi:10.1021/jm00225a001
(1976)
Doi:10.1021/jo00870a002
(1976)
Doi:10.1002/macp.1976.021770111
(1976)
Diazo reactions with unsaturated compounds: VIII. Reaction of 1,3-butadiene and isoprene with aromatic and aliphatic-aromatic triazenes in the presence of sulfur(IV) oxide

Doi:10.1007/s11176-005-0016-5
(2004)
Photoexcitation of iron-allyl complexes (η⁵:η¹-C₅H₄CH₂CH₂PPh₂)Fe(CO)(η¹-CH₂CR=CH₂) (R = H, CH₃) which contains a tethered phosphine ligand

Doi:10.1016/S0022-328X(97)00280-5
(1997)

Article Doi