| Full text | |
| Author(s): |
Total Authors: 3
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| Affiliation: | [1] Univ Sao Paulo, Inst Chem, Sao Paulo - Brazil
Total Affiliations: 1
|
| Document type: | Journal article |
| Source: | ORGANIC & BIOMOLECULAR CHEMISTRY; v. 18, n. 28, p. 5458-5465, JUL 28 2020. |
| Web of Science Citations: | 0 |
| Abstract | |
Coixspirolactams, spiro{[}oxindole-gamma-lactones], are found in adlay seeds and exhibit anticancer activity. A novel synthetic methodology was developed to enable an easy access to (+/-)-coixspirolactam A and a large number of new coixspirolactams in excellent overall yields. The exquisite exploitation of formamide reactivity was essential for the construction of oxindole and lactone scaffolds. (AU) | |
| FAPESP's process: | 19/10762-1 - Development of a synthetic platform using carbamoyl radicals: application of the formamide in the synthesis of heterocyclic compounds |
| Grantee: | Leandro Helgueira de Andrade |
| Support Opportunities: | Regular Research Grants |
| FAPESP's process: | 17/02854-8 - Synthetic applications of carbamoyl radicals via photocatalysis |
| Grantee: | Leandro Helgueira de Andrade |
| Support Opportunities: | Regular Research Grants |