Fluorination 2017
DOI: 10.1007/978-981-10-1855-8_15-1
|View full text |Cite
|
Sign up to set email alerts
|

Functionalization of Alkynes for Preparing Alkenyl Fluorides

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

1
0

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 66 publications
0
1
0
Order By: Relevance
“…Common 18 F radiosynthesis precursors include carbon electrophiles (R–X, where X = halides or pseudo halides) and organometals (R–M, where M = B, Sn, or Si) (Scheme a) . Alkynes are ubiquitous in organic synthesis, and unlike common 18 F radiosynthesis precursors such as RX and RM, alkynes are generally chemically inert under most reaction conditions (acids, bases, oxidants, and reductants) . Therefore, alkynes are ideal 18 F radiosynthesis precursors, especially for late-stage radiofluorinations.…”
mentioning
confidence: 99%
“…Common 18 F radiosynthesis precursors include carbon electrophiles (R–X, where X = halides or pseudo halides) and organometals (R–M, where M = B, Sn, or Si) (Scheme a) . Alkynes are ubiquitous in organic synthesis, and unlike common 18 F radiosynthesis precursors such as RX and RM, alkynes are generally chemically inert under most reaction conditions (acids, bases, oxidants, and reductants) . Therefore, alkynes are ideal 18 F radiosynthesis precursors, especially for late-stage radiofluorinations.…”
mentioning
confidence: 99%