ChemInform Abstract: STEROIDE 28. MITT. DARST. VON STEROIDHORMON‐ANALOGEN AUS 2,3BETA‐IMINO‐5ALPHA‐ANDROSTANOL‐(17BETA) UND 3ALPHA‐CHLOR‐2BETA‐AMINO‐5ALPHA‐ANDROSTANOL‐(17BETA)

Ponsold, K.; Preibsch, Wolfgang

doi:10.1002/chin.197134358

Chemischer Informationsdienst. Organische Chemie

1971

DOI: 10.1002/chin.197134358

|View full text |Cite

ChemInform Abstract: STEROIDE 28. MITT. DARST. VON STEROIDHORMON‐ANALOGEN AUS 2,3BETA‐IMINO‐5ALPHA‐ANDROSTANOL‐(17BETA) UND 3ALPHA‐CHLOR‐2BETA‐AMINO‐5ALPHA‐ANDROSTANOL‐(17BETA)

K. Ponsold¹,

Wolfgang Preibsch²

Abstract: Das Epoxid (I) gibt bei der Umsetzung mit Na‐azid in Äthylenglykol das Hydroxyazid (IIa) (92% Ausbeute), dessen Tosylat (IIb) durch Reaktion mit Naboranat in das Androstandiol‐Derivat (III) (90%) übergeführt wird.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Publication Types

Select...

Relationship

Self Cite0

Independent0

Authors

Journals

Cited by 0 publications

References 1 publication

Supporting

Mentioning

Contrasting

Order By: Relevance

No citations

Set email alert for when this publication receives citations?

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

ChemInform Abstract: STEROIDE 28. MITT. DARST. VON STEROIDHORMON‐ANALOGEN AUS 2,3BETA‐IMINO‐5ALPHA‐ANDROSTANOL‐(17BETA) UND 3ALPHA‐CHLOR‐2BETA‐AMINO‐5ALPHA‐ANDROSTANOL‐(17BETA)

Abstract: Das Epoxid (I) gibt bei der Umsetzung mit Na‐azid in Äthylenglykol das Hydroxyazid (IIa) (92% Ausbeute), dessen Tosylat (IIb) durch Reaktion mit Naboranat in das Androstandiol‐Derivat (III) (90%) übergeführt wird.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About