A Base‐Labile Protecting Group (Fluorenylmethoxycarbonyl) for the 5′‐Hydroxy Function of Nucleosides
Author:
Affiliation:
1. MRC Laboratory of Molecular Biology Cambridge United Kingdom
2. Institute of Organic Chemistry, University of Lausanne Lausanne Switzerland
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc0204s00
Reference37 articles.
1. E. Atherton R.C. Sheppard 1989 IRL Press Oxford
2. Solid Phase Synthesis of DNA Under a Non-Depurinating Condition with a Base Labile 5′-Protecting Group (Fmoc) Using Phosphiteamidite Approach
3. Allyl as internucleotide protecting group in DNA synthesis to be cleaved off by ammonia
4. Brown T. Pritchard C.E. Turner G. andSalisbury S.A.1989.A new base‐stable linker for solid‐phase oligonucleotide synthesis.J. Chem. Soc. Chem. Commun.891‐893.
5. CV. Total synthesis of the structural gene for an alanine transfer ribonucleic acid from yeast. Chemical synthesis of an icosadeoxyribonucleotide corresponding to the nucleotide sequence 31 to 50
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