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

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

126 Scopus citations

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
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 - 1 Apr 1992
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

Access to Document

10.1021/jo00034a005

Cite this

@article{ae29f299b1354541bd2cb7dbc22ed3bd,

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",

month = apr,

day = "1",

doi = "10.1021/jo00034a005",

language = "English",

volume = "57",

pages = "2215--2217",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "8",

}

TY - JOUR

T1 - Controlled Molecular Aggregation. 1. Cyclic Trimerization via Hydrogen Bonding

AU - Zimmerman, Steven C.

AU - Duerr, Brook F.

PY - 1992/4/1

Y1 - 1992/4/1

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.

UR - http://www.scopus.com/inward/record.url?scp=5644290035&partnerID=8YFLogxK

U2 - 10.1021/jo00034a005

DO - 10.1021/jo00034a005

M3 - Article

AN - SCOPUS:5644290035

SN - 0022-3263

VL - 57

SP - 2215

EP - 2217

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 8

ER -

Controlled Molecular Aggregation. 1. Cyclic Trimerization via Hydrogen Bonding

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this