A rearrangement-based approach to secondary difluorophosphonates

Afshan H Butt , Jonathan Percy, Neil S Spencer

Research output: Contribution to journalArticle

40 Citations (Scopus)

Abstract

[3,3]-Claisen rearrangements allowed the conversion of a readily available allylic difluorophosphonate to nucleic acid and inositol phosphate-related products via epoxide cyclisation or ring closing metathesis respectively.
LanguageEnglish
Pages1691-1692
Number of pages2
JournalChemical Communications
Volume2000
Issue number17
Early online date23 Aug 2000
DOIs
Publication statusPublished - 2000

Fingerprint

Inositol Phosphates
Cyclization
Epoxy Compounds
Nucleic acids
Nucleic Acids
Phosphates

Keywords

  • rearrangements
  • allylic difluorophosphonate
  • nucleic acid
  • epoxide cyclisation
  • secondary difluorophosphonates

Cite this

Butt , Afshan H ; Percy, Jonathan ; Spencer, Neil S. / A rearrangement-based approach to secondary difluorophosphonates. In: Chemical Communications. 2000 ; Vol. 2000, No. 17. pp. 1691-1692.
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A rearrangement-based approach to secondary difluorophosphonates. / Butt , Afshan H; Percy, Jonathan; Spencer, Neil S.

In: Chemical Communications, Vol. 2000, No. 17, 2000, p. 1691-1692.

Research output: Contribution to journalArticle

TY - JOUR

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AU - Butt , Afshan H

AU - Percy, Jonathan

AU - Spencer, Neil S

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KW - rearrangements

KW - allylic difluorophosphonate

KW - nucleic acid

KW - epoxide cyclisation

KW - secondary difluorophosphonates

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DO - 10.1039/b005110l

M3 - Article

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SP - 1691

EP - 1692

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T2 - Chemical Communications

JF - Chemical Communications

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