Main NMR Characteristics of Synthetic (25r)-5α-furostanes-Reference-Cited by-同舟云学术

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Main NMR Characteristics of Synthetic (25r)-5α-furostanes

Published:2001-01 Issue:1 Volume:2001 Page:34-35
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Iglesias-Arteaga Martin A.¹,Martínez Carlos Pérez¹,Manchado Francisco Coll¹

Affiliation:

1. Laboratorio de Productos Naturales, Facultad de Química, Universidad de La Habana, La Habana 10 400, Cuba

Abstract

The assignment of 13C signals of synthetic (25R)-5α -furostanes together with the main 1H characteristics of the furostane side chain are presented. The main effects on chemical shifts due to conversion of ring F into an open chain are briefly discussed.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823401103168208

Reference9 articles.

1. Synthesis of (25R)-5α-Spirostan-2α,3α,6β-triol Triacetate#

2. Synthesis and Characterization of (25R)-2α,3α-Epoxy-5α-Spirostan-12,23-Dione

3. Aluminum Chloride-Catalyzed Opening of the Steroidal Sapogenin Spiroketal System1

4. 543. Steroidal sapogenins: the isomerisation of normal to iso-sapogenins

Cited by 2 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. Reductive desymmetrization of steroid dimers;Steroids;2021-12

2. Synthesis of diamino-furostan sapogenins and their use as scaffolds for positioning peptides in a preorganized form;Tetrahedron;2008-05

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