86794-55-0

Upstream product

• 98-88-4 benzoyl chloride 
• 25819-78-7 (Z)-6β-methoxy-3α,5-cyclo-5α-cholest-22-ene 
• 25819-80-1 (22E)-6β-methoxy-3α,5-cyclo-5α-cholest-22-ene 
• 51231-28-8 (3R)-3-((3S,10R,13R,17R)-10,13-dimethyl-3-((tetrahydro-2H-pyran-2-yl)oxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)butanal 
• 79190-31-1 3-[(tetrahydro-2H-pyran-2-yl)oxy]-24-norchol-5-en-23-ol 
• 86834-13-1 cholesta-5,22-diene-3β,23-diol 3-THP ether 
• 81677-31-8 (3S,8S,9S,10R,13R,14S,17R)-17-((R)-3-Hydroxy-1,5-dimethyl-hex-5-enyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 
• 81677-31-8 (23S)-cholesta-5,25-diene-3β,23-diol 
• 34347-28-9 22-dehydrocholesterol 
• 57597-07-6 24-norchola-5,22-dien-3β-ol 
• 19462-13-6 3β-acetoxy-5-cholenic acid 
• 27241-03-8 (3β,23R)-cholest-5-ene-3,23-diol 
• 81677-29-4 (23S)-cholesta-5,25-diene-3β,23-diol dibenzoate 
• 82542-89-0 tetrahydro-2-{[(3β)-24-norchola-5,22-dien-3-yl]oxy}-2H-pyran 

Relevant academic research and scientific papers

Further Investigations of the Stereochemistry of Electrophilic-Addition Reactions of the Steroidal C-22 Double Bond

Three kinds of electrophilic addition reactions, viz. peracid epoxidation, hydroboration, and iodoacetoxylation, of both the trans- and cis-isomers of 6β-methoxy-3α,5-cyclo-5α-cholest-22-enes (1) and (2) were examined.The observed stereoselectivity can be