Enantioselective total synthesis of aspidophytine

[1] A NEW EFFICIENT TOTAL SYNTHESIS OF VINDOROSINE AND VINDOLINE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (07) : 961 - 967

[2] [Anonymous], 1967, J CHEM SOC CHEM COMM

[3] SYNTHESIS OF 5,6,7-TRIMETHOXY-2,3-DIHYDROINDOLE AND 6,7-DIMETHOXYINDOLE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1959, 24 (07) : 917 - 919

[4] BUCHI G, 1971, J AM CHEM SOC, V93, P3299

[5] METHODS FOR INDOLE ALKALOID SYNTHESIS - A STUDY OF THE COMPATIBILITY OF THE INDOLE 2,3-QUINODIMETHANE STRATEGY FOR THE SYNTHESIS OF 16-METHOXY-SUBSTITUTED ASPIDOSPERMA-TYPE ALKALOIDS - SYNTHESIS OF (+)- AND (-)-16-METHOXYTABERSONINE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (07) : 2242 - 2248

[6] CAVA MP, 1963, CHEM IND-LONDON, P1875

[7] CAVA MP, 1963, CHEM IND-LONDON, P1242

[8] X-ray crystal and NMR structure of a highly reactive bidentate 1,2-diamine-OsO4 complex, formally a 20-electron outer valence shell species. Mechanistic implications for the 1,2-diamine-accelerated dihydroxylation of olefins by OsO4 [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (33) : 7851 - 7852

[9] Corey EJ, 1998, ANGEW CHEM INT EDIT, V37, P1987, DOI 10.1002/(SICI)1521-3773(19980817)37:15<1986::AID-ANIE1986>3.0.CO

[10] 2-Z

[1] A NEW EFFICIENT TOTAL SYNTHESIS OF VINDOROSINE AND VINDOLINE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (07) : 961 - 967

[2] [Anonymous], 1967, J CHEM SOC CHEM COMM

[3] SYNTHESIS OF 5,6,7-TRIMETHOXY-2,3-DIHYDROINDOLE AND 6,7-DIMETHOXYINDOLE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1959, 24 (07) : 917 - 919

[4] BUCHI G, 1971, J AM CHEM SOC, V93, P3299

[5] METHODS FOR INDOLE ALKALOID SYNTHESIS - A STUDY OF THE COMPATIBILITY OF THE INDOLE 2,3-QUINODIMETHANE STRATEGY FOR THE SYNTHESIS OF 16-METHOXY-SUBSTITUTED ASPIDOSPERMA-TYPE ALKALOIDS - SYNTHESIS OF (+)- AND (-)-16-METHOXYTABERSONINE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (07) : 2242 - 2248

[6] CAVA MP, 1963, CHEM IND-LONDON, P1875

[7] CAVA MP, 1963, CHEM IND-LONDON, P1242

[8] X-ray crystal and NMR structure of a highly reactive bidentate 1,2-diamine-OsO4 complex, formally a 20-electron outer valence shell species. Mechanistic implications for the 1,2-diamine-accelerated dihydroxylation of olefins by OsO4 [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (33) : 7851 - 7852

[9] Corey EJ, 1998, ANGEW CHEM INT EDIT, V37, P1987, DOI 10.1002/(SICI)1521-3773(19980817)37:15<1986::AID-ANIE1986>3.0.CO

[10] 2-Z