Constructing 24(23→22)-abeo-Cholestane from Tigogenin in a 20(22→23)-abeo-Way via a PhI(OAc)2-mediated Favorskii Rearrangement-Reference-Cited by-同舟云学术

Constructing 24(23→22)-abeo-Cholestane from Tigogenin in a 20(22→23)-abeo-Way via a PhI(OAc)2-mediated Favorskii Rearrangement

Published:2017-04-03 Issue:8 Volume:82 Page:4402-4406
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jiang Xiao-Ling¹,Shi Yong¹^ORCID,Tian Wei-Sheng¹

Affiliation:

1. CAS Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b03043

Reference30 articles.

1. Structure of a novel 22-homo-23-norcholestane trisaccharide from Ornithogalum saundersiae

2. Three novel rearranged cholestane glycosides from Ornithogalum saundersiae bulbs and their cytostatic activities on leukemia HL-60 and MOLT-4 cells

3. Novel cholestane glycosides from the bulbs of Ornithogalum saundersiae and their cytostatic activity on leukemia HL-60 and MOLT-4 cells

4. Saundersiosides C–H, rearranged cholestane glycosides from the bulbs of Ornithogalum saundersiae and their cytostatic activity on HL-60 cells

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Favorskii Rearrangement (Extend to Rings);Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

2. Rearrangement Reactions;Applied Organic Chemistry;2020-12-11

3. Sequential Nucleophilic Arylation/Ring-Contractive Rearrangement of N-Alkoxylactams;Organic Letters;2020-12-02

4. A.E.Favorskii’s scientific legacy in modern organic chemistry: prototropic acetylene – allene isomerization and the acetylene zipper reaction;Russian Chemical Reviews;2020-01-01

5. Synthesis of 18-Demethoxy Analogues of the Aglycon of Saundersiosides A and B, Based on a Cascade Process;Asian Journal of Organic Chemistry;2017-06-07