Controlled Molecular Aggregation. 1. Cyclic Trimerization via Hydrogen Bonding

Steven C. Zimmerman; Brook F. Duerr

doi:10.1021/jo00034a005

Controlled Molecular Aggregation. 1. Cyclic Trimerization via Hydrogen Bonding

Steven C. Zimmerman, Brook F. Duerr

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Vapor pressure osmometric and ¹H NMR dilution studies of quinolone 7, isoquinolone 8, and pyrido[4,3-g]quinolinedione 1, indicate that 1 forms an extremely robust cyclic trimer in solution.

Original language	English (US)
Pages (from-to)	2215-2217
Number of pages	3
Journal	Journal of Organic Chemistry
Volume	57
Issue number	8
DOIs	https://doi.org/10.1021/jo00034a005
State	Published - Apr 1 1992

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Organic Chemistry

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10.1021/jo00034a005

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title = "Controlled Molecular Aggregation. 1. Cyclic Trimerization via Hydrogen Bonding",

abstract = "Vapor pressure osmometric and 1H NMR dilution studies of quinolone 7, isoquinolone 8, and pyrido[4,3-g]quinolinedione 1, indicate that 1 forms an extremely robust cyclic trimer in solution.",

author = "Zimmerman, {Steven C.} and Duerr, {Brook F.}",

year = "1992",

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language = "English (US)",

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journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

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AU - Duerr, Brook F.

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N2 - Vapor pressure osmometric and 1H NMR dilution studies of quinolone 7, isoquinolone 8, and pyrido[4,3-g]quinolinedione 1, indicate that 1 forms an extremely robust cyclic trimer in solution.

AB - Vapor pressure osmometric and 1H NMR dilution studies of quinolone 7, isoquinolone 8, and pyrido[4,3-g]quinolinedione 1, indicate that 1 forms an extremely robust cyclic trimer in solution.

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Controlled Molecular Aggregation. 1. Cyclic Trimerization via Hydrogen Bonding

Abstract

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