scholarly journals Synthetic Studies on Nodulisporic Acids with Multi-substituted Indole Skeleton

2019 ◽  
Vol 77 (8) ◽  
pp. 845-848
Author(s):  
Takuya Okada
Keyword(s):  
Synthetic Studies ◽  
Nodulisporic Acids

scholarly journals Indole Diterpene Synthetic Studies. Total Synthesis of (+)-Nodulisporic Acid F and Construction of the Heptacyclic Cores of (+)-Nodulisporic Acids A and B and (-)-Nodulisporic Acid D.

ChemInform ◽  
2007 ◽  
Vol 38 (48) ◽  
Author(s):  
Amos B. III Smith ◽  
Akin H. Davulcu ◽  
Young Shin Cho ◽  
Kazuyuki Ohmoto ◽  
Laszlo Kuerti ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Synthetic Studies ◽  
Nodulisporic Acids

scholarly journals Indole Diterpene Synthetic Studies: Development of a Second-Generation Synthetic Strategy for (+)-Nodulisporic Acids A and B.

ChemInform ◽  
2007 ◽  
Vol 38 (43) ◽  
Author(s):  
Amos B. III Smith ◽  
Laszlo Kuerti ◽  
Akin H. Davulcu ◽  
Young Shin Cho ◽  
Kazuyuki Ohmoto
Keyword(s):  
Second Generation ◽  
Synthetic Strategy ◽  
Synthetic Studies ◽  
Nodulisporic Acids

Indole Diterpene Synthetic Studies:  Development of a Second-Generation Synthetic Strategy for (+)-Nodulisporic Acids A and B

2007 ◽  
Vol 72 (13) ◽  
pp. 4611-4620 ◽  
Author(s):  
Amos B. Smith ◽  
László Kürti ◽  
Akin H. Davulcu ◽  
Young Shin Cho ◽  
Kazuyuki Ohmoto
Keyword(s):  
Second Generation ◽  
Synthetic Strategy ◽  
Synthetic Studies ◽  
Nodulisporic Acids

Indole Diterpene Synthetic Studies. Total Synthesis of (+)-Nodulisporic Acid F and Construction of the Heptacyclic Cores of (+)-Nodulisporic Acids A and B and (−)-Nodulisporic Acid D

2007 ◽  
Vol 72 (13) ◽  
pp. 4596-4610 ◽  
Author(s):  
Amos B. Smith ◽  
Akin H. Davulcu ◽  
Young Shin Cho ◽  
Kazuyuki Ohmoto ◽  
László Kürti ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Synthetic Studies ◽  
Nodulisporic Acids

Synthetic studies toward inducamide C

2021 ◽  
Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry
Keyword(s):  
Natural Product ◽  
Structural Revision ◽  
Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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