Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Murugesan, Thangamani"'
Autor:
Rajendran, Aarthi, Murugesan, Thangamani, Chinnasamy, Narmatha, Rao, Gurudharshini Balaji, Muthuraj, Iswarya, Krishnamoorthy, Mounisuhitha
Publikováno v:
AIP Conference Proceedings; 2023, Vol. 2790 Issue 1, p1-8, 8p
Publikováno v:
RSC Advances. 11:14980-14985
A tin(IV) chloride promoted (3 + 2) annulation of trans-2-aroyl-3-styrylcyclopropane-1,1-dicarboxylates with nitriles is reported. The transformation involves the Lewis acid assisted formation of 1,5-dipolar intermediates from the cyclopropane dicarb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32f386d55562803a9421de01f750adcf
https://doi.org/10.1039/d1ra01194d
https://doi.org/10.1039/d1ra01194d
Publikováno v:
The Journal of Organic Chemistry. 86:1172-1177
The reaction of aroyl-substituted donor–acceptor (D–A) cyclopropanes with two equivalents of 1-naphthylamines in the presence of a catalytic amount of scandium(III) triflate provides access to dibe...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c46257fe10316e0522baafa8666431b1
https://doi.org/10.1021/acs.joc.0c02105
https://doi.org/10.1021/acs.joc.0c02105
Publikováno v:
Organicbiomolecular chemistry. 20(15)
The chemistry of donor-acceptor (D-A) cyclopropanes containing alkyl donors has been scantily investigated. In the present work, we have synthesized new D-A cyclopropanes containing arylethyl donors and explored their reactivity in the presence of Le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f257b2c8dd6f5beb6debb9f7a8ccb80d
https://pubmed.ncbi.nlm.nih.gov/35343561
https://pubmed.ncbi.nlm.nih.gov/35343561
Publikováno v:
RSC advances. 11(25)
A tin(iv) chloride promoted (3 + 2) annulation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7f25a764df5249ab34568b19c92f52e
https://pubmed.ncbi.nlm.nih.gov/35424056
https://pubmed.ncbi.nlm.nih.gov/35424056
Publikováno v:
The Journal of organic chemistry. 86(1)
The reaction of aroyl-substituted donor-acceptor (D-A) cyclopropanes with two equivalents of 1-naphthylamines in the presence of a catalytic amount of scandium(III) triflate provides access to dibenzo[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b8a06ab6fa0d2dc5608524f87baaa50
https://pubmed.ncbi.nlm.nih.gov/33236912
https://pubmed.ncbi.nlm.nih.gov/33236912
Publikováno v:
The Journal of organic chemistry. 83(2)
The ring-opening reaction of trans-2-aroyl-3-styrylcyclopropane-1,1-dicarboxylates was investigated with different Lewis acids. With SnCl4, the cyclopropane dicarboxylates afforded cyclopentene derivatives through ring opening followed by cyclization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46f5298adced2b535120d1b5aa5467fc
https://pubmed.ncbi.nlm.nih.gov/29251929
https://pubmed.ncbi.nlm.nih.gov/29251929
Publikováno v:
Technology in Cancer Research & Treatment; March 2018, Vol. 17 Issue: 1