Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Butyl cinnamate"'
Publikováno v:
Hemijska Industrija, Vol 69, Iss 1, Pp 37-42 (2015)
This study deals with synthesis of methyl cinnamate, butyl cinnamate, and p-methoxy methyl cinnamate and testing of their in vitro antimicrobial activity. Antimicrobial activity was examined towards 29 microorganisms using microdilution method. It
Externí odkaz:
https://doaj.org/article/ace12c892ff14188bb7990c1f852e9a6
Publikováno v:
Hemijska Industrija, Vol 69, Iss 1, Pp 37-42 (2015)
Hemijska industrija (2015) 69(1):37-42
Hemijska industrija (2015) 69(1):37-42
This study deals with synthesis of methyl cinnamate, butyl cinnamate, and p-methoxy methyl cinnamate and testing of their in vitro antimicrobial activity. Antimicrobial activity was examined towards 29 microorganisms using microdilution method. It is
Publikováno v:
Food and Chemical Toxicology. 45:S49-S52
A toxicologic and dermatologic review of butyl cinnamate when used as a fragrance ingredient is presented.
Publikováno v:
Organic Process Research & Development. 8:477-481
A continuous microflow system was developed with efficient catalyst recycling for a Mizoroki−Heck reaction of iodobenzene with butyl acrylate, using a low-viscosity ionic liquid ([bmim]NTf2) as the...
Publikováno v:
Tetrahedron: Asymmetry. 11:2437-2441
The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyr
Autor:
Rodrigo M. Bastos, Ricardo R. Bonfim, Luciano M. Lião, Silvio Cunha, Ana Monteiro, Kelly S. Alencar
Publikováno v:
Química Nova v.26 n.3 2003
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Repositório Institucional da UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA
Química Nova, Vol 26, Iss 3, Pp 425-427 (2003)
Química Nova, Volume: 26, Issue: 3, Pages: 425-427, Published: MAY 2003
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Repositório Institucional da UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA
Química Nova, Vol 26, Iss 3, Pp 425-427 (2003)
Química Nova, Volume: 26, Issue: 3, Pages: 425-427, Published: MAY 2003
p. 425-427 Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2014-01-08T11:25:16Z No. of bitstreams: 1 Silvio Cunha.pdf: 256831 bytes, checksum: 8af84ad113a675205ebf5bc6fbf4ba01 (MD5) Made available in DSpace on 2014-01-08T11:25:16Z (GMT). No.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdcf9c2d27a6a880d6677d7694b22b72
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422003000300022
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422003000300022
Autor:
Silvio Cunha, Luciano M. Lião, Ricardo R. Bonfim, Rodrigo M. Bastos, Ana Paula M. Monteiro, Kelly S. Alencar
Publikováno v:
Química Nova, Vol 26, Iss 3, Pp 425-427 (2003)
An experiment for the synthesis of isobutylene from tert-butanol dehydratation using oxalic acid as catalyst, followed by preparations of tert-butyl benzoate and tert-butyl cinnamate is described. The synthesis are simple, requiring two periods of 4
Autor:
Cunha, Silvio do Desterro, Lião, Luciano M., Bonfim, Ricardo R., Bastos, Rodrigo M., Monteiro, Ana Paula de Melo, Alencar, Kelly S.
Publikováno v:
Repositório Institucional da UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA
p. 425-427 Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2014-01-08T11:25:16Z No. of bitstreams: 1 Silvio Cunha.pdf: 256831 bytes, checksum: 8af84ad113a675205ebf5bc6fbf4ba01 (MD5) Made available in DSpace on 2014-01-08T11:25:16Z (GMT). No.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::3cc251d089ce8fbd009f5ed793ea9656
http://repositorio.ufba.br/ri/handle/ri/14295
http://repositorio.ufba.br/ri/handle/ri/14295
Publikováno v:
TETRAHEDRON-ASYMMETRY. 5(10)
A model for the stereoselective conjugate addition of lithium (α-methylbenzyl) benzylamide, to t-butyl cinnamate has been devised, using molecular modelling techniques.
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