Multicomponent Ligation of Steroids: Creating Diversity at the Linkage Moiety of Bis-spirostanic Conjugates by Ugi Reactions

Author:

Pérez-Labrada Karell123,Méndez Yanira1,Brouard Ignacio3,Rivera Daniel G.1

Affiliation:

1. Center for Natural Products Study, Faculty of Chemistry, University of Havana, Zapata y G, 10400, La Habana, Cuba

2. Institute of Pharmacy and Food, University of Havana, San Lázaro y L, 10400, La Habana, Cuba

3. Instituto de Productos Naturales y Agrobiología-C.S.I.C., Avda. Astrofísico Francisco Sánchez 3, 38206 La Laguna, Tenerife, Spain

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,General Medicine

Cited by 12 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. A review on steroid dimers: 2011–2019;Steroids;2020-12

2. Diversity-oriented synthesis of 17-spirosteroids;Beilstein Journal of Organic Chemistry;2020-04-28

3. Mesoscale Assembly of Bisteroidal Esters from Terephthalic Acid;Molecules;2020-03-08

4. One-Pot Parallel Synthesis of 5-(Dialkylamino)tetrazoles;ACS Combinatorial Science;2019-08-22

5. Steroid diversification by multicomponent reactions;Beilstein Journal of Organic Chemistry;2019-06-06

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