Bromine-lithium exchange on gem-dibromoalkenes part 1: batch vs microflow conditions-Reference-Cited by-同舟云学术

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Bromine-lithium exchange on gem-dibromoalkenes part 1: batch vs microflow conditions

Published:2020-02-14 Issue:1 Volume:10 Page:139-143
ISSN:2062-249X
Container-title:Journal of Flow Chemistry
language:en
Short-container-title:J Flow Chem

Author:

Picard Baptiste,Pérez Katia,Lebleu Thomas,Vuluga Daniela,Burel Fabrice,Harrowven David C.,Chataigner Isabelle,Maddaluno Jacques,Legros Julien^ORCID

Funder

Labex SynOrg

Interreg

Consejería de Educación, Juventud y Deporte, Comunidad de Madrid

Association Instituts Carnot

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Fluid Flow and Transfer Processes,Chemistry (miscellaneous)

Link

http://link.springer.com/content/pdf/10.1007/s41981-019-00057-6.pdf

Reference20 articles.

1. Knorr R (2004) Alkylidenecarbenes, Alkylidenecarbenoids,† and competing species: which is responsible for Vinylic Nucleophilic substitution, [1 + 2] Cycloadditions, 1,5-CH insertions, and the Fritsch−Buttenberg−Wiechell rearrangement? Chem. Rev. 104(9):3795–3850. https://doi.org/10.1021/cr030616h

2. Capriati V, Florio S (2010) Anatomy of long-lasting love affairs with Lithium Carbenoids: past and present status and future prospects. Chem. Eur. J. 16(14):4152–4162. https://doi.org/10.1002/chem.200902870

3. Chelucci G (2012) Synthesis and metal-catalyzed reactions of gem-Dihalovinyl systems. Chem. Rev. 112(3):1344–1462. https://doi.org/10.1021/cr200165q

4. Harada T, Katsuhira T, Hattori K, Oku A (1994) Stereochemistry in Carbenoid formation by bromine/Lithium and bromine/zinc exchange reactions of gem-Dibromo compounds. Tetrahedron 50(27):7987–8002. https://doi.org/10.1016/S0040-4020(01)85284-4

5. Fürst R, Rinner U (2013) Synthesis of an advanced intermediate of the Jatrophane Diterpene Pl-4: a Dibromide coupling approach. J. Organomet. Chem. 78(17):8748–8758. https://doi.org/10.1021/jo401480t

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