One-pot efficient synthesis of 13(R),14(R)-epoxy-17β-methyl-20(S)-hydroxyl-18-nor-pregna-4-en-3-one via a tandem epoxidation-rearrangement-epoxidation reaction sequence-Reference-Cited by-同舟云学术

One-pot efficient synthesis of 13(R),14(R)-epoxy-17β-methyl-20(S)-hydroxyl-18-nor-pregna-4-en-3-one via a tandem epoxidation-rearrangement-epoxidation reaction sequence

Published:2013-12 Issue:14 Volume:78 Page:1332-1338
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Feng Shu-Xiao^ORCID,Zhang Ya-Dong

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

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4. A new ginsengenin containing an oxacyclopentane-ring isolated from the acid hydrolysate of total ginsenosides;Guan;Chin Chem Lett,2013

5. Starfish saponins III. A novel steroidal sapogenin, 17β-methyl-3β,6α-dihydroxy-18-nor-5α-cholesta-9(11),13-dien-23-one, from the starfish Astropecten aurantiacus;De Simone;Tetrahedron Lett,1979

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