Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Silva Jr., Luiz F."'
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 17, Iss 1, Pp 200-205 (2006)
The rearrangement of beta,gamma-unsaturated esters, such as 2-(3,4-dihydronaphthalen-1-yl)-propionic acid ethyl ester, with thallium trinitrate (TTN) in acetic acid leads to 3-indan-1-yl-2-methyl-3-oxo-propionic acid ethyl ester in good yield, throug
Externí odkaz:
https://doaj.org/article/2d41bb114f544517b846f9c05fb23ecf
Autor:
Ferraz Helena M. C., Silva Jr. Luiz F.
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 12, Iss 4, Pp 548-551 (2001)
The reaction of some cis-2-decalones with TTN in CH2Cl2 at room temperature was investigated. The ring contraction reactions occurred in good yields, however the regio- and diastereoselectivity were low. The effect of the alkyl groups in the regioche
Externí odkaz:
https://doaj.org/article/617b714aaa6d429aadb50bb87d114ea1
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 12, Iss 5, Pp 680-684 (2001)
The reaction of a series of 1-tetralones with thallium trinitrate supported on Montmorillonite K-10 clay led to products of ring contraction (methyl indan-1-carboxylates) and/or alpha-oxidation (2-methoxy-1-tetralones), in variable yields.
Externí odkaz:
https://doaj.org/article/b8ce447799a945a1ad0224b7b33ae7c1
Akademický článek
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Publikováno v:
Journal of the Brazilian Chemical Society, Volume: 24, Issue: 9, Pages: 1414-1419, Published: SEP 2013
Journal of the Brazilian Chemical Society v.24 n.9 2013
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society v.24 n.9 2013
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Iodine-catalyzed Prins cyclization of homoallylic alcohols and ketones was investigated. Anhydrous conditions and inert atmosphere are not required in this metal-free protocol. The reaction of 2-(3,4-dihydronaphthalen-1-yl)propan-1-ol with six alipha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f99e3a06e0d6f95c7fd4f738f4e7dd94
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013000900004&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013000900004&lng=en&tlng=en
Publikováno v:
Journal of Organic Chemistry; 11/2/2018, Vol. 83 Issue 21, p13604-13611, 8p
Publikováno v:
Química Nova, Volume: 31, Issue: 4, Pages: 781-787, Published: 2008
The reaction of ten cis-octalins and cis-octalones with thallium trinitrate (TTN) leads to different products, depending mainly on the substitution pattern of the substrate. Functionalized cis-hydrindanes were obtained from the reaction of 1,2,3,4,4a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::27342fdadf6650b7b66fffbe49b970ff
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422008000400014&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422008000400014&lng=en&tlng=en
Publikováno v:
Journal of the Brazilian Chemical Society, Volume: 18, Issue: 6, Pages: 1281-1284, Published: 2007
a,a-Dichloro-cyclic aryl ketones were obtained treating a methanolic solution of the corresponding ketone with commercial bleach at ambient conditions in yields varying from 61 to 92%. Electron-donating and -withdrawing groups in the starting ketone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::f55b3973f69adda778fc711e3d4b60fe
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000600026&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000600026&lng=en&tlng=en
Publikováno v:
Journal of the Brazilian Chemical Society v.18 n.6 2007
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
a,a-Dichloro-cyclic aryl ketones were obtained treating a methanolic solution of the corresponding ketone with commercial bleach at ambient conditions in yields varying from 61 to 92%. Electron-donating and -withdrawing groups in the starting ketone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::f55b3973f69adda778fc711e3d4b60fe
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000600026
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000600026
Publikováno v:
Journal of Organic Chemistry; 11/17/2017, Vol. 82 Issue 22, p11787-11791, 5p