Explore: Allyl Halides
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Books Results
Source: The Open Library
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Search results from The Open Library
1Allyl chloride and other allyl halides
By Shell Chemical Corporation.
“Allyl chloride and other allyl halides” Metadata:
- Title: ➤ Allyl chloride and other allyl halides
- Author: Shell Chemical Corporation.
- Language: English
- Number of Pages: Median: 136
- Publisher: shell chemical corporation
- Publish Date: 1949
- Publish Location: New York
“Allyl chloride and other allyl halides” Subjects and Themes:
- Subjects: Allyl halides
Edition Identifiers:
- The Open Library ID: OL6065234M
- Online Computer Library Center (OCLC) ID: 1397799
- Library of Congress Control Number (LCCN): 50001458
Access and General Info:
- First Year Published: 1949
- Is Full Text Available: Yes
- Is The Book Public: No
- Access Status: Borrowable
Online Access
Downloads Are Not Available:
The book is not public therefore the download links will not allow the download of the entire book, however, borrowing the book online is available.
Online Borrowing:
- Borrowing from Open Library: Borrowing link
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2Secondary deuterium isotope effects in allylic rearrangements
By Gailerd Lee Korver
“Secondary deuterium isotope effects in allylic rearrangements” Metadata:
- Title: ➤ Secondary deuterium isotope effects in allylic rearrangements
- Author: Gailerd Lee Korver
- Language: English
- Number of Pages: Median: 62
- Publish Date: 1969
“Secondary deuterium isotope effects in allylic rearrangements” Subjects and Themes:
- Subjects: Rearrangements (Chemistry) - Deuterium - Allyl halides
Edition Identifiers:
- The Open Library ID: OL16727223M
Access and General Info:
- First Year Published: 1969
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
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3Molecular orbital studies of heterosubstituted allyl and vinyl carbanions
By Nathan Harris
“Molecular orbital studies of heterosubstituted allyl and vinyl carbanions” Metadata:
- Title: ➤ Molecular orbital studies of heterosubstituted allyl and vinyl carbanions
- Author: Nathan Harris
- Language: English
- Number of Pages: Median: 58
- Publish Date: 1991
“Molecular orbital studies of heterosubstituted allyl and vinyl carbanions” Subjects and Themes:
- Subjects: Allyl halides - Chemistry - Molecular orbitals - Vinyl polymers
Edition Identifiers:
- The Open Library ID: OL14695807M
Access and General Info:
- First Year Published: 1991
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
Online Marketplaces
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4The migratory group in the para-Claisen rearrangement
By Robert Wagner Ledeen
“The migratory group in the para-Claisen rearrangement” Metadata:
- Title: ➤ The migratory group in the para-Claisen rearrangement
- Author: Robert Wagner Ledeen
- Language: English
- Number of Pages: Median: 55
- Publish Date: 1954
“The migratory group in the para-Claisen rearrangement” Subjects and Themes:
- Subjects: Claisen condensation - Allyl halides
Edition Identifiers:
- The Open Library ID: OL14311649M
Access and General Info:
- First Year Published: 1954
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
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Wiki
Source: Wikipedia
Wikipedia Results
Search Results from Wikipedia
Allyl halide
Allyl halides are organic halides containing an allyl group. Allyl halides include: Allyl chloride Allyl bromide Allyl iodide Allyl fluoride [Wikidata]
Allyl iodide
verification] Allyl iodide can be synthesized from allyl alcohol and methyl iodide on triphenyl phosphite, Finkelstein reaction on allyl halides, or by the
Transition metal allyl complex
synthesis, as allyl halides readily undergo Wurtz coupling. Mercury and tin allyl halides appear to avoid this side-reaction. Benzyl and allyl ligands often
Allyl chloride
Allyl chloride is the organic compound with the formula CH2=CHCH2Cl. This colorless liquid is insoluble in water but soluble in common organic solvents
Enolate
enolates via allyl halide to generate Oulema melanopus Besides reacting with epoxides, aza enolates can also react with alkyl halides (or allyl halides as depicted
Allyl cyanide
CH2=CHCH2Br + CuCN → CH2=CHCH2CN + CuBr Other allyl halides may be used for this reaction including allyl iodide as done by A. Rinne and B. Tollens in
Allyl bromide
Allyl bromide (3-bromopropene) is an organic halide. It is an alkylating agent used in synthesis of polymers, pharmaceuticals, perfumes and other organic
Organotin chemistry
aryltin(II) halides. Organotin compounds can be synthesised by numerous methods. Classic is the reaction of a Grignard reagent with tin halides for example
Nozaki–Hiyama–Kishi reaction
scope was extended by the same authors to include vinyl halides or triflates and aryl halides. It was observed that the success of the reaction depended
Organonickel chemistry
simple allyl complexes. Allyl halides react with Ni(CO)4 to form pi-allyl complexes, (allyl)2Ni2Cl2. These compounds in turn are sources of allyl nucleophiles