Journal
ORGANIC LETTERS
Volume 24, Issue 31, Pages 5825-5828Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c02367
Keywords
-
Categories
Funding
- National Nature Science Foundation of China [21961043, 22161049]
- Yunnan University
Ask authors/readers for more resources
The novel congeners 5 alpha,6-dihydro of veragranines A and B, with unprecedented hexacyclic skeleton and potent analgesic effects, were synthesized in six steps from hecogenin acetate. This method provides a quick access to the hexacyclic skeleton and can be utilized for preparing other D-ring modified congeners.
The 5 alpha,6-dihydro congeners of veragranines A and B, two steroidal alkaloids with an unprecedented hexacyclic skeleton and potent analgesic effects, were synthesized from hecogenin acetate within six steps. This work enables quick access to the hexacyclic skeleton and is amendable to prepare other D -ring-modified congeners.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available