Cleavage of steroidal α-hydroxy acetals with methylmagnesium iodide
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930000783
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1. Rearrangement of a steroidal α-hydroxyacetal: a convenient new method for the introduction of a 5α-methyl group into the steroid nucleus
2. Neighbouring group participation in the cleavage of steroidal α-hydroxyacetals
3. Intramolecular condensation of steroidal α-acetoxy-ketones
4. Optical Rotatory Dispersion Studies. XXXVI.1 α-Haloketones (Part 7).2 Demonstration of Boat Form in the Bromination of 2α-Methylcholestan-3-one3,4
5. The Epoxidation of 1-Acetoxycyclohexene and the Rearrangement of 1-Acetoxy-1,2-epoxycyclohexane1
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