| Full text | |
| Author(s): |
Total Authors: 2
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| Affiliation: | [1] Univ Estadual Campinas, Inst Chem, BR-13083970 Campinas, SP - Brazil
Total Affiliations: 1
|
| Document type: | Journal article |
| Source: | ORGANIC LETTERS; v. 17, n. 10, p. 2490-2493, MAY 15 2015. |
| Web of Science Citations: | 16 |
| Abstract | |
A novel, divergent strategy toward the synthesis of beta-branched (and linear) Carbonyl Compounds is developed by taking advantage Of alkylidene isoxazol-5-ones as key building blocks. The yields obtained range from good to excellent, therefore making the described methods attractive options for building such molecules. (AU) | |
| FAPESP's process: | 13/09680-4 - H-Bond catalysis for the synthesis of chiral molecules |
| Grantee: | Igor Dias Jurberg |
| Support Opportunities: | Regular Research Grants |
| FAPESP's process: | 14/15718-7 - Exploring 5-isoxazolones for the synthesis of beta-aminoacids |
| Grantee: | Naylil Malagutti Rodrigues Capreti |
| Support Opportunities: | Scholarships in Brazil - Scientific Initiation |