Highly Stereoselective One-Pot Procedure To Prepare Bis- and Tris-chalcogenide Alkenes via Addition of Disulfides and Diselenides to Terminal Alkynes-Reference-Cited by-同舟云学术

Highly Stereoselective One-Pot Procedure To Prepare Bis- and Tris-chalcogenide Alkenes via Addition of Disulfides and Diselenides to Terminal Alkynes

Published:2005-05-25 Issue:13 Volume:70 Page:5257-5268
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Moro Angélica Venturini¹,Nogueira Cristina W.¹,Barbosa Nilda B. V.¹,Menezes Paulo Henrique¹,da Rocha João Batista Teixeira¹,Zeni Gilson¹

Affiliation:

1. Laboratório de Síntese, Reatividade, Avaliação Farmacológica e Toxicológica de Organocalcogênios, CCNE, UFSM, Santa Maria, Rio Grande do Sul, Brazil 97105-900, and Departamento de Química Fundamental, UFPE, Recife, PE, Brazil 50670-901

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo050448o

Reference59 articles.

1. Synthesis of ketene phenyltelluroacetals by a Wittig-Horner route

2. Chalcogen electrophile induced rearrangement of 1-alkynyltrialkyl borates: controlled syntheses of trisubstituted olefins from 1-alkynes

3. Stereoselective sp2–sp2 bond formation via Negishi cross-coupling of vinylic tellurides and 2-heteroarylzinc chlorides

4. Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-couplingElectronic supplementary information (ESI) available: spectroscopic data for all new compounds as well as detailed experimental procedures. See http://www.rsc.org/suppdata/ob/b4/b401059k/

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