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dihydroindole alkaloids (22) 22
chemistry, organic (14) 14
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Synthesis, ISSN 0039-7881, 07/2019, Volume 51, Issue 14, pp. 2737 - 2758
Journal Article
Organic Letters, ISSN 1523-7060, 06/2017, Volume 19, Issue 12, pp. 3167 - 3170
A uniformly strategic total synthesis of Aspidosperma alkaloids (+)-vincadifformine, (−)-quebrachamine, (+)-aspidospermidine, (−)-aspidospermine,... 
INTRAMOLECULAR SCHMIDT REACTION | DL-ASPIDOSPERMIDINE | ENANTIOSELECTIVE SYNTHESES | CHEMISTRY, ORGANIC | BIOMIMETIC ALKALOID SYNTHESES | GENERAL ENTRY | INDOLE ALKALOIDS | QUATERNARY CARBON CENTERS | DIHYDROINDOLE ALKALOIDS | ASPIDOSPERMA ALKALOIDS | FORMAL TOTAL SYNTHESIS
Journal Article
Organic Letters, ISSN 1523-7060, 06/2018, Volume 20, Issue 12, pp. 3647 - 3650
The first enantioselective total synthesis of (−)-vallesine via a strategy that features a late-stage regioselective C17-oxidation followed by a highly... 
BISCHLER-NAPIERALSKI REACTION | CONCISE TOTAL SYNTHESES | NATURAL-PRODUCTS | DL-ASPIDOSPERMIDINE | CHEMISTRY, ORGANIC | GENERAL ENTRY | C-H BORYLATION | PHOTO-ISOMERIZATION | DIHYDROINDOLE ALKALOIDS | QUEBRACHAMINE | ASPIDOSPERMA ALKALOIDS | Alkaloids | Cyclization | Oxidation-Reduction | Stereoisomerism | Molecular Structure | Indoles - chemistry | Boron Compounds
Journal Article
Organic Letters, ISSN 1523-7060, 08/2011, Volume 13, Issue 15, pp. 4116 - 4119
Detailed investigations on one of the key steps of the superacidic fluorination of Vinca alkaloids that is the origin of C20′ activation are reported. While... 
(+)-CATHARANTHINE | INDOLE | STEREOCONTROLLED TOTAL-SYNTHESIS | LEUROSINE | ANHYDROVINBLASTINE | CHEMISTRY, ORGANIC | VINBLASTINE | HF-SBF5 | DIHYDROINDOLE ALKALOIDS | DERIVATIVES | ACCESS | Vinca Alkaloids - chemistry | Molecular Structure | Acids - chemistry | Dimerization | Halogenation | Hydrogen-Ion Concentration
Journal Article
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, ISSN 0037-9980, 02/2009, Volume 67, Issue 2, pp. 123 - 133
Journal Article
Journal of the Chemical Society of Pakistan, ISSN 0253-5106, 2011, Volume 33, Issue 6, pp. 905 - 915
Vindoline is a major alkaloid from the leaves of Vinca roseus Linn. (Catharanthus roseus G. Don) Apocynaceae. Chemically vindoline lacks physiological activity... 
PERFORMANCE LIQUID-CHROMATOGRAPHY | MULTIPLE SHOOT CULTURES | VINCA ALKALOIDS | ONE-POT SYNTHESIS | CATHARANTHUS-ROSEUS | STEREOCONTROLLED TOTAL-SYNTHESIS | INDOLE ALKALOIDS | DIHYDROINDOLE ALKALOIDS | CHEMISTRY, MULTIDISCIPLINARY | NEAR-ULTRAVIOLET LIGHT | ELECTROCHEMICAL SYNTHESIS
Journal Article
Heterocycles, ISSN 0385-5414, 07/2007, Volume 71, Issue 7, pp. 1553 - 1563
Aromatic electrophilic substitution reactions of the monomer alkaloid vindoline resulted in new derivatives substituted on ring A. Halogene-, nitro-, amino-... 
Nitration | Bisindole Alkaloid | Vindoline | Aromatic Electrophilic Substitution | Halogenation | REARRANGEMENT | VINCA ALKALOIDS | INDOLE | nitration | VINCRISTINE | CHEMISTRY, ORGANIC | VINBLASTINE | halogenation | bisindole alkaloid | aromatic electrophilic substitution | vindoline | DIHYDROINDOLE ALKALOIDS
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 2007, Volume 48, Issue 38, pp. 6731 - 6734
Journal Article
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