Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters

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Standard

Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters. / Lysén, M.; Madden, M.; Kristensen, Jesper Langgaard; Vedsø, P.; Zöllner, C.; Begtrup, M.

In: Synthesis, No. 20, 17.10.2006, p. 3478-3484.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lysén, M, Madden, M, Kristensen, JL, Vedsø, P, Zöllner, C & Begtrup, M 2006, 'Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters', Synthesis, no. 20, pp. 3478-3484. https://doi.org/10.1055/s-2006-950239

APA

Lysén, M., Madden, M., Kristensen, J. L., Vedsø, P., Zöllner, C., & Begtrup, M. (2006). Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters. Synthesis, (20), 3478-3484. https://doi.org/10.1055/s-2006-950239

Vancouver

Lysén M, Madden M, Kristensen JL, Vedsø P, Zöllner C, Begtrup M. Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters. Synthesis. 2006 Oct 17;(20):3478-3484. https://doi.org/10.1055/s-2006-950239

Author

Lysén, M. ; Madden, M. ; Kristensen, Jesper Langgaard ; Vedsø, P. ; Zöllner, C. ; Begtrup, M. / Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters. In: Synthesis. 2006 ; No. 20. pp. 3478-3484.

Bibtex

@article{26282cdac3644cabad6c5025da5e26f3,
title = "Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters",
abstract = "1-Fluoro-, 1-chloro- and 1-cyanonaphthalene were lithiated and then borylated at the 2-position. The 1-substituted naphthaleneboronic esters were cross-coupled with aryl halides to give 2-aryl-1-fluoro-, 2-aryl-1-chloro- and 2-aryl-1-cyanonaphthalenes. The 2-aryl-1-cyano- and 2-aryl-1-fluoronaphthalenes were reacted with n-butyllithium or lithium morpholide to give new benzophenanthridine derivatives.",
author = "M. Lys{\'e}n and M. Madden and Kristensen, {Jesper Langgaard} and P. Veds{\o} and C. Z{\"o}llner and M. Begtrup",
year = "2006",
month = "10",
day = "17",
doi = "10.1055/s-2006-950239",
language = "English",
pages = "3478--3484",
journal = "Synthesis",
issn = "0039-7881",
publisher = "GeorgThieme Verlag",
number = "20",

}

RIS

TY - JOUR

T1 - Synthesis, cross-coupling, and anionic cyclization of ortho-substituted naphthaleneboronic esters

AU - Lysén, M.

AU - Madden, M.

AU - Kristensen, Jesper Langgaard

AU - Vedsø, P.

AU - Zöllner, C.

AU - Begtrup, M.

PY - 2006/10/17

Y1 - 2006/10/17

N2 - 1-Fluoro-, 1-chloro- and 1-cyanonaphthalene were lithiated and then borylated at the 2-position. The 1-substituted naphthaleneboronic esters were cross-coupled with aryl halides to give 2-aryl-1-fluoro-, 2-aryl-1-chloro- and 2-aryl-1-cyanonaphthalenes. The 2-aryl-1-cyano- and 2-aryl-1-fluoronaphthalenes were reacted with n-butyllithium or lithium morpholide to give new benzophenanthridine derivatives.

AB - 1-Fluoro-, 1-chloro- and 1-cyanonaphthalene were lithiated and then borylated at the 2-position. The 1-substituted naphthaleneboronic esters were cross-coupled with aryl halides to give 2-aryl-1-fluoro-, 2-aryl-1-chloro- and 2-aryl-1-cyanonaphthalenes. The 2-aryl-1-cyano- and 2-aryl-1-fluoronaphthalenes were reacted with n-butyllithium or lithium morpholide to give new benzophenanthridine derivatives.

UR - http://www.scopus.com/inward/record.url?scp=33750585356&partnerID=8YFLogxK

U2 - 10.1055/s-2006-950239

DO - 10.1055/s-2006-950239

M3 - Journal article

AN - SCOPUS:33750585356

SP - 3478

EP - 3484

JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 20

ER -

ID: 45438484