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Journal Article
PLoS ONE, ISSN 1932-6203, 02/2018, Volume 13, Issue 2, p. e0192113
Journal Article
Catalysts, ISSN 2073-4344, 06/2018, Volume 8, Issue 6, p. 250
The synthesis of the two 7,8-epoxides of carvone has been attained using organocatalysis in a two-step synthetic route through a bromoester intermediate. Among... 
Epoxidation | Proline | Carvone | Organocatalysis | Aminocatalysis | Epoxide | OXIDATION | ENANTIOPURE | carvone | CHEMISTRY, PHYSICAL | organocatalysis | proline | ALKENES | epoxidation | OLEFINS | EFFICIENT | DERIVATIVES | aminocatalysis | epoxide | C-H | Stereoselectivity | Organic chemistry | Synthesis | Bromination | Amino acids | Oxidation | Catalysis
Journal Article
MOLECULES, ISSN 1420-3049, 06/2019, Volume 24, Issue 11, p. 2120
Recently, the methylene-cycloakylacetate (MCA) scaffold has been reported as a potential pharmacophore for neurite outgrowth activity. In this work, natural... 
neurotrophic | ENT-HALIMANOLIDES | ACID | ent-halimic acid | CLERODANE DITERPENOIDS | MINOR DITERPENOIDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | halimanes | methylene-cycloalkylacetate | MCA | HYMENAEA-COURBARIL | HALIMANE-TYPE DITERPENOIDS | CHEMISTRY, MULTIDISCIPLINARY | PLECTRANTHUS-ORNATUS | ABSOLUTE-CONFIGURATION | HALIMIUM-VISCOSUM | CONSTITUENTS
Journal Article
ISSN 0265-0568, 9/2018, Volume 35, Issue 9, pp. 955 - 991
Covering: 1970 to 2017 Diterpenes with a halimane skeleton constitute a small group of natural products that can be biogenetically considered as being between... 
Journal Article
Natural Product Reports, ISSN 0265-0568, 01/2018, Volume 35, Issue 9, pp. 955 - 991
Covering: 1970 to 2017 Diterpenes with a halimane skeleton constitute a small group of natural products that can be biogenetically considered as being between... 
Tuberculosis | Natural products | Nomenclature | Germination | Diterpenes | Biomarkers | Biosynthesis | Repellency | Aquatic insects | Anticancer properties
Journal Article
Natural Product Reports, ISSN 0265-0568, 09/2018, Volume 35, Issue 9, pp. 955 - 991
Journal Article
Natural Product Communications, ISSN 1934-578X, 2017, Volume 12, Issue 5, pp. 667 - 670
Sclareol has been employed as starting material for the synthesis of several advanced intermediates towards the synthesis of highly ring B oxygenated labdanes.... 
Labdanes | Pregalauterone | Forskolin | Sclareol | Leopersin | CHEMISTRY, MEDICINAL | DITERPENE FORSKOLIN | FOOD SCIENCE & TECHNOLOGY | (+/-)-FORSKOLIN | ADENYLATE-CYCLASE | Colforsin - chemical synthesis | Diterpenes - chemical synthesis | Molecular Structure
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