Release of DNA oligonucleotides and their conjugates from controlled-pore glass under thermolytic conditions.

about

Release of DNA oligonucleotides and their conjugates from controlled-pore glass under thermolytic conditions.

Item

http://www.wikidata.org/entity/Q46196437

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年学术文章

@wuu

2008年学术文章

@zh-cn

2008年学术文章

@zh-hans

2008年学术文章

@zh-my

2008年学术文章

@zh-sg

2008年學術文章

@yue

2008年學術文章

@zh

2008年學術文章

@zh-hant

name

Release of DNA oligonucleotide ...... under thermolytic conditions.

@en

Release of DNA oligonucleotide ...... under thermolytic conditions.

@nl

type

Item

label

Release of DNA oligonucleotide ...... under thermolytic conditions.

@en

Release of DNA oligonucleotide ...... under thermolytic conditions.

@nl

prefLabel

Release of DNA oligonucleotide ...... under thermolytic conditions.

@en

Release of DNA oligonucleotide ...... under thermolytic conditions.

@nl

P1476

Release of DNA oligonucleotide ...... under thermolytic conditions.

@en

P2093

Andrzej Grajkowski

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

Darón I Freedberg

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

Jacek Cieślak

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

Jon S Kauffman

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

Robert J Duff

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

Scott Norris

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

Serge L Beaucage

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

P2860

Cleavage of oligodeoxyribonucleotides from controlled-pore glass supports and their rapid deprotection by gaseous amines

Studies on the role of tetrazole in the activation of phosphoramidites

Stepwise synthesis of oligodeoxyribonucleotides on an insoluble polymer support

Advances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach

A new and versatile approach to the preparation of valuable deoxynucleoside 3′-phosphite intermediates

Solid-phase oligosaccharide synthesis and combinatorial carbohydrate libraries.

Automated synthesis of oligosaccharides as a basis for drug discovery.

Automated synthesis of peptides.

The 3-(N-tert-butylcarboxamido)-1-propyl group as an attractive phosphate/thiophosphate protecting group for solid-phase oligodeoxyribonucleotide synthesis.

Thermolytic properties of 3-(2-pyridyl)-1-propyl and 2-[N-methyl-N-(2-pyridyl)]aminoethyl phosphate/thiophosphate protecting groups in solid-phase synthesis of oligodeoxyribonucleotides.

P304

Unit 3.17

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

P31

scholarly article

P356

10.1002/0471142700.NC0317S35

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

P478

Chapter 3

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

P577

2008-12-01T00:00:00Z

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

P5875

23666730

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

P698

19085983

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