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1 / 3-Dipolar cycloaddition / Proton NMR / Nuclear magnetic resonance spectroscopy / Chemistry / Nuclear magnetic resonance / Spectroscopy


Copper–phenanthroline catalysts for regioselective synthesis of pyrrolo[3′,4′:3,4]pyrrolo[1,2-a]furoquinolines/phenanthrolines and of pyrrolo[1,2-a]phenanthrolines under mild conditions
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City

Madison / Eigendorf / Cambridge / New Delhi / Sharma / Mondal / /

Company

Gothelf A. S. / Henkel / Bruker AXS Inc. / Dias L. C. / Girgis A. S. / Creative Commons / /

Country

United States / United Kingdom / /

Currency

pence / /

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Facility

The Cambridge Crystallographic Data Centre / Indian Institute of Chemical Biology / Cambridge Crystallographic Data Centre / /

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IndustryTerm

metal / cycloaddition protocol / chemical and pharmacological points / catalytic systems / final cycloaddition products / structural networks / /

Organization

Cambridge Crystallographic Data Centre / Indian Institute of Chemical Biology / Beilstein-Institut / Council of Scientific and Industrial Research / Department of Chemistry / /

Person

Nirup B. Mondal / Prakas R. Maulik / B. Achari / Yogesh P. Bharitkar / Sandip Kundu / Shyamal Mondal / Abhijit Hazra / /

Position

Editor / rt rt rt rt / rt / Experimental General / representative / Corresponding author / Ex-Emeritus Scientist / /

Product

Sc / /

ProvinceOrState

South Dakota / Wisconsin / New Brunswick / /

PublishedMedium

the Beilstein Journal / /

Technology

X-ray / optimized protocol / condensation / microwave / cycloaddition protocol / pdf / /

URL

http /

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