ChemInform Abstract: Synthetic Studies of Erythromycins. Part 2. Enantiospecific Synthesis of a C-10-C-13 Segment of Erythronolide A from D-Ribose. Synthetic Studies of Erythromycins. Part 3. Total Synthesis of Erythronolide A Through (9S)-9-Dihydroerythr

1986 ◽  
Vol 17 (36) ◽  
Author(s):  
M. KINOSHITA ◽  
M. ARAI ◽  
K. TOMOOKA ◽  
M. NAKATA ◽  
N. OHSAWA
2003 ◽  
Vol 86 (12) ◽  
pp. 3908-3938 ◽  
Author(s):  
Amos B. Smith ◽  
Haifeng Cui

1978 ◽  
Vol 26 (10) ◽  
pp. 3150-3153 ◽  
Author(s):  
SANGWON KIM ◽  
YUKIHIDE BANDO ◽  
NOBUKO TAKAHASHI ◽  
ZENICHI HORII

Synlett ◽  
2020 ◽  
Author(s):  
Fu-She Han ◽  
Dong-Xing Tan

AbstractIn this account, recent progress on the synthetic studies of several monoterpene indole alkaloids, (±)-mersicarpine, misassigned (±)-tronoharine, and (±)-leuconodines D and E, is summarized. Specifically, the rationale for the design and development of the Lewis acid catalyzed SN1-type substitution and formal [3+3] cycloaddition reaction of indol-2-yl carbinols, and the Pd-catalyzed aerobic oxidative intramolecular Heck cross-coupling of indolyl amides tethered with a terminal olefin functionality, are emphasized. These key reactions set the basis for the rapid construction of the fused ring skeleton containing an all-carbon quaternary center at the indol-2-yl position.1 Introduction2 Synthetic Study of (±)-Mersicarpine3 Synthetic Study of the Misassigned (±)-Tronoharine4 Study of the Asymmetric Reaction of Indol-2-yl Carbinols5 Synthetic Study of (±)-Leuconodines D and E6 Conclusion


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