Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate
Ozonolysis of maleopimaric anhydride methyl ester in the presence of tetracyanoethylene led to an epoxide and an ozonide. Ozonolysis of the trimethyl fumaropimarate, followed by treatment with Me2S, led to an epoxide, a diene, a keto-acid and an allylic oxidation product. Some of the compounds obtai...
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| Format: | Article |
| Language: | English |
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Sociedade Brasileira de Química
2000-01-01
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| Series: | Journal of the Brazilian Chemical Society |
| Subjects: | |
| Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000100011 |
| _version_ | 1819054880568901632 |
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| author | Hess Sonia C. Farah Maria I. S. Eguchib Silvia Y. Imamura Paulo M. |
| author_facet | Hess Sonia C. Farah Maria I. S. Eguchib Silvia Y. Imamura Paulo M. |
| author_sort | Hess Sonia C. |
| collection | DOAJ |
| description | Ozonolysis of maleopimaric anhydride methyl ester in the presence of tetracyanoethylene led to an epoxide and an ozonide. Ozonolysis of the trimethyl fumaropimarate, followed by treatment with Me2S, led to an epoxide, a diene, a keto-acid and an allylic oxidation product. Some of the compounds obtained were active against Staphylococcus aureus, Bacillus subtilis and Micrococcus luteus. |
| first_indexed | 2024-12-21T12:58:39Z |
| format | Article |
| id | doaj.art-2844375d13a94ad8b2e312ecb90b5be8 |
| institution | Directory Open Access Journal |
| issn | 0103-5053 |
| language | English |
| last_indexed | 2024-12-21T12:58:39Z |
| publishDate | 2000-01-01 |
| publisher | Sociedade Brasileira de Química |
| record_format | Article |
| series | Journal of the Brazilian Chemical Society |
| spelling | doaj.art-2844375d13a94ad8b2e312ecb90b5be82022-12-21T19:03:14ZengSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society0103-50532000-01-011115963Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarateHess Sonia C.Farah Maria I. S.Eguchib Silvia Y.Imamura Paulo M.Ozonolysis of maleopimaric anhydride methyl ester in the presence of tetracyanoethylene led to an epoxide and an ozonide. Ozonolysis of the trimethyl fumaropimarate, followed by treatment with Me2S, led to an epoxide, a diene, a keto-acid and an allylic oxidation product. Some of the compounds obtained were active against Staphylococcus aureus, Bacillus subtilis and Micrococcus luteus.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000100011Pinus elliottiis' rosinoxidationmaleopimaric anhydride methyl estertrimethyl fumaropimarate |
| spellingShingle | Hess Sonia C. Farah Maria I. S. Eguchib Silvia Y. Imamura Paulo M. Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate Journal of the Brazilian Chemical Society Pinus elliottiis' rosin oxidation maleopimaric anhydride methyl ester trimethyl fumaropimarate |
| title | Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate |
| title_full | Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate |
| title_fullStr | Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate |
| title_full_unstemmed | Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate |
| title_short | Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate |
| title_sort | synthetic studies with pinus elliottiis rosin derivatives oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate |
| topic | Pinus elliottiis' rosin oxidation maleopimaric anhydride methyl ester trimethyl fumaropimarate |
| url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000100011 |
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