ChemInform Abstract: SYNTHETIC STUDIES TOWARD COMPLEX DITERPENOIDS. 16. A NOVEL SYNTHETIC ROUTE TO O THE CARBOCYCLIC SKELETA OF STEMODIN AND STEMARIN BY ACID-CATALYZED INTRAMOLECULAR C-ALKYLATION AND REARRANGEMENT REACTIONS

1985 ◽  
Vol 16 (33) ◽  
Author(s):  
P. R. KANJILAL ◽  
M. SARKAR ◽  
S. K. PATRA ◽  
S. GHOSH ◽  
U. R. GHATAK
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


Tetrahedron ◽  
1997 ◽  
Vol 53 (5) ◽  
pp. 1593-1606 ◽  
Author(s):  
Hideharu Suzuki ◽  
Chiemie Iwata(nee Miyaga) ◽  
Katsumi Sakurai ◽  
Kazuhiko Tokumoto ◽  
Hiroko Takahashi ◽  
...  

2005 ◽  
Vol 53 (7) ◽  
pp. 743-746 ◽  
Author(s):  
Fen-Er Chen ◽  
Hui-Qing Jia ◽  
Xu-Xiang Chen ◽  
Hui-Fang Dai ◽  
Bin Xie ◽  
...  

1975 ◽  
Vol 40 (13) ◽  
pp. 2011-2012 ◽  
Author(s):  
T. Fukuyama ◽  
L. V. Dunkerton ◽  
M. Aratani ◽  
Y. Kishi

2017 ◽  
Vol 15 (16) ◽  
pp. 3519-3527 ◽  
Author(s):  
Thamina Akther ◽  
Md. Monarul Islam ◽  
Shofiur Rahman ◽  
Paris E. Georghiou ◽  
Taisuke Matsumoto ◽  
...  

Acid catalyzed rearrangement reactions of [2.n]metacyclophan-1-enes afford new chiral [n.1]metacyclophanes; DFT calculations have been used to estimate the energy-minimized structures of the metacyclophanes.


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