Standard
Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF. / Petersen, Trine P; Larsen, Anders Foller; Ritzén, Andreas; Ulven, Trond.
In:
Journal of Organic Chemistry, Vol. 78, No. 8, 2013, p. 4190-4195.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Petersen, TP, Larsen, AF, Ritzén, A
& Ulven, T 2013, '
Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF',
Journal of Organic Chemistry, vol. 78, no. 8, pp. 4190-4195.
https://doi.org/10.1021/jo400390tAPA
Petersen, T. P., Larsen, A. F., Ritzén, A.
, & Ulven, T. (2013).
Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF.
Journal of Organic Chemistry,
78(8), 4190-4195.
https://doi.org/10.1021/jo400390tVancouver
Petersen TP, Larsen AF, Ritzén A
, Ulven T.
Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF.
Journal of Organic Chemistry. 2013;78(8):4190-4195.
https://doi.org/10.1021/jo400390tAuthor
Petersen, Trine P ; Larsen, Anders Foller ; Ritzén, Andreas ; Ulven, Trond. / Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF. In: Journal of Organic Chemistry. 2013 ; Vol. 78, No. 8. pp. 4190-4195.
Bibtex
@article{ac01670bdb564a17af5627a92a754909,
title = "Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF",
abstract = "A safe, practical, and scalable continuous flow protocol for the in situ generation of dimethylamine from DMF followed by nucleophilic aromatic substitution of a broad range of aromatic and heteroaromatic halides is reported.",
author = "Petersen, {Trine P} and Larsen, {Anders Foller} and Andreas Ritz{\'e}n and Trond Ulven",
year = "2013",
doi = "10.1021/jo400390t",
language = "English",
volume = "78",
pages = "4190--4195",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "8",
}
RIS
TY - JOUR
T1 - Continuous Flow Nucleophilic Aromatic Substitution with Dimethylamine Generated in Situ by Decomposition of DMF
AU - Petersen, Trine P
AU - Larsen, Anders Foller
AU - Ritzén, Andreas
AU - Ulven, Trond
PY - 2013
Y1 - 2013
N2 - A safe, practical, and scalable continuous flow protocol for the in situ generation of dimethylamine from DMF followed by nucleophilic aromatic substitution of a broad range of aromatic and heteroaromatic halides is reported.
AB - A safe, practical, and scalable continuous flow protocol for the in situ generation of dimethylamine from DMF followed by nucleophilic aromatic substitution of a broad range of aromatic and heteroaromatic halides is reported.
U2 - 10.1021/jo400390t
DO - 10.1021/jo400390t
M3 - Journal article
VL - 78
SP - 4190
EP - 4195
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
SN - 0022-3263
IS - 8
ER -
