Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5226861 | Tetrahedron | 2009 | 9 Pages |
Abstract
Five new C-C bonded steroidal homodimers derived from deoxycholic acid, pregnenolone, and progesterone were synthesized by an olefin metathesis reaction assisted by microwave heating. Microwave improved the yield and accelerated the reaction allowing the use of less catalyst with good results (2.5 mol %). Due to the bulky nature of the steroidal skeleton the more favorable E-dimers were formed as the sole or major products depending on the linker length.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Valeria C. Edelsztein, Pablo H. Di Chenna, Gerardo Burton,