Curran, DP and Luo, Z and Degenkolb, P
(1998)
'Propylene spaced' allyl tin reagents: A new class of fluorous tin reagents for allylations under radical and metal-catalyzed conditions.
Bioorganic and Medicinal Chemistry Letters, 8 (17).
2403 - 2408.
ISSN 0960-894X
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Abstract
A new generation of propylene-spaced fluorous allyltin reagents [(Rf(CH2)3)3SnCH2CH=CH2] is described. These succeed in radical allylations where their lower homologs (ethylene-spaced) fail, and they provide improved performance in transition metal catalyzed allylations. The reagents and byproducts are readily separated by simple fluorous-organic liquid-liquid or solid-liquid extractions.
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Details
Item Type: |
Article
|
Status: |
Published |
Creators/Authors: |
Creators | Email | Pitt Username | ORCID  |
---|
Curran, DP | curran@pitt.edu | CURRAN | | Luo, Z | | | | Degenkolb, P | | | |
|
Date: |
8 September 1998 |
Date Type: |
Publication |
Journal or Publication Title: |
Bioorganic and Medicinal Chemistry Letters |
Volume: |
8 |
Number: |
17 |
Page Range: |
2403 - 2408 |
DOI or Unique Handle: |
10.1016/s0960-894x(98)00435-1 |
Schools and Programs: |
Dietrich School of Arts and Sciences > Chemistry |
Refereed: |
Yes |
ISSN: |
0960-894X |
MeSH Headings: |
Aldehydes--chemical synthesis; Aldehydes--chemistry; Alkenes; Catalysis; Fluorides; Indicators and Reagents; Metals; Organotin Compounds--chemical synthesis; Organotin Compounds--chemistry; Structure-Activity Relationship |
PubMed ID: |
9873550 |
Date Deposited: |
28 Jul 2014 19:11 |
Last Modified: |
22 Jun 2021 12:56 |
URI: |
http://d-scholarship.pitt.edu/id/eprint/22506 |
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