ChemInform Abstract: Synthesis of B‐Ring‐Modified Steroids Through BF<sub>3</sub>‐Promoted Rearrangement/Substitution of 6β‐Hydroxy‐5,19‐cyclosteroids.

Kranz, Darius P.; Chiha, Slim; Greffen, Aike Meier zu; Neudoerfl, Joerg‐Martin; Schmalz, Hans‐Guenther

doi:10.1002/chin.201247200

ChemInform

2012

DOI: 10.1002/chin.201247200

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ChemInform Abstract: Synthesis of B‐Ring‐Modified Steroids Through BF₃‐Promoted Rearrangement/Substitution of 6β‐Hydroxy‐5,19‐cyclosteroids.

Darius P. Kranz¹,

Slim Chiha²,

Aike Meier zu Greffen³

et al.

Abstract: Me3Si‐allyl as the nucleophile gives the highest yield of the rearranged alcohol (XIII) after hydrolysis.

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ChemInform Abstract: Synthesis of B‐Ring‐Modified Steroids Through BF₃‐Promoted Rearrangement/Substitution of 6β‐Hydroxy‐5,19‐cyclosteroids.

Abstract: Me3Si‐allyl as the nucleophile gives the highest yield of the rearranged alcohol (XIII) after hydrolysis.

Cited by 0 publications

References 1 publication

No citations

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ChemInform Abstract: Synthesis of B‐Ring‐Modified Steroids Through BF3‐Promoted Rearrangement/Substitution of 6β‐Hydroxy‐5,19‐cyclosteroids.

Abstract: Me3Si‐allyl as the nucleophile gives the highest yield of the rearranged alcohol (XIII) after hydrolysis.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Synthesis of B‐Ring‐Modified Steroids Through BF₃‐Promoted Rearrangement/Substitution of 6β‐Hydroxy‐5,19‐cyclosteroids.