Microwave-assisted synthesis of naphthalenemonoimides and N-desymmetrized naphthalenediimides

K Tambara; N Ponnuswamy; G Hennrich; Gheorghe D Pantos

doi:10.1021/jo200177s

Microwave-assisted synthesis of naphthalenemonoimides and N-desymmetrized naphthalenediimides

K Tambara, N Ponnuswamy, G Hennrich, Gheorghe D Pantos

Department of Chemistry

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

47 Citations (SciVal)

Abstract

Naphthalenemonoimides and N-desymmetrized naphthalenediimides were synthesized using a stepwise microwave-assisted protocol. The steric and electronic properties of aliphatic amines determined the outcome of the reactions, while in the amino acid series their ability to solubilize the naphthalene dianhydride starting material was crucial. Molecular modeling was used to rationalize the observed selectivity.

Original language	English
Pages (from-to)	3338-3347
Number of pages	10
Journal	Journal of Organic Chemistry
Volume	76
Issue number	9
DOIs	https://doi.org/10.1021/jo200177s
Publication status	Published - 6 May 2011

Bibliographical note

Tambara, Koujiro Ponnuswamy, Nandhini Hennrich, Gunther Pantos, G. Dan

Access to Document

10.1021/jo200177s

Cite this

@article{65dc46e5a827492a914bc8b275d6ff65,

title = "Microwave-assisted synthesis of naphthalenemonoimides and N-desymmetrized naphthalenediimides",

abstract = "Naphthalenemonoimides and N-desymmetrized naphthalenediimides were synthesized using a stepwise microwave-assisted protocol. The steric and electronic properties of aliphatic amines determined the outcome of the reactions, while in the amino acid series their ability to solubilize the naphthalene dianhydride starting material was crucial. Molecular modeling was used to rationalize the observed selectivity.",

author = "K Tambara and N Ponnuswamy and G Hennrich and Pantos, {Gheorghe D}",

note = "Tambara, Koujiro Ponnuswamy, Nandhini Hennrich, Gunther Pantos, G. Dan",

year = "2011",

month = may,

day = "6",

doi = "10.1021/jo200177s",

language = "English",

volume = "76",

pages = "3338--3347",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "9",

}

TY - JOUR

T1 - Microwave-assisted synthesis of naphthalenemonoimides and N-desymmetrized naphthalenediimides

AU - Tambara, K

AU - Ponnuswamy, N

AU - Hennrich, G

AU - Pantos, Gheorghe D

N1 - Tambara, Koujiro Ponnuswamy, Nandhini Hennrich, Gunther Pantos, G. Dan

PY - 2011/5/6

Y1 - 2011/5/6

N2 - Naphthalenemonoimides and N-desymmetrized naphthalenediimides were synthesized using a stepwise microwave-assisted protocol. The steric and electronic properties of aliphatic amines determined the outcome of the reactions, while in the amino acid series their ability to solubilize the naphthalene dianhydride starting material was crucial. Molecular modeling was used to rationalize the observed selectivity.

AB - Naphthalenemonoimides and N-desymmetrized naphthalenediimides were synthesized using a stepwise microwave-assisted protocol. The steric and electronic properties of aliphatic amines determined the outcome of the reactions, while in the amino acid series their ability to solubilize the naphthalene dianhydride starting material was crucial. Molecular modeling was used to rationalize the observed selectivity.

UR - http://www.scopus.com/inward/record.url?scp=79955562847&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1021/jo200177s

U2 - 10.1021/jo200177s

DO - 10.1021/jo200177s

M3 - Article

SN - 0022-3263

VL - 76

SP - 3338

EP - 3347

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 9

ER -

Microwave-assisted synthesis of naphthalenemonoimides and N-desymmetrized naphthalenediimides

Abstract

Bibliographical note

Access to Document

Other files and links

Fingerprint

Cite this