Aluminum Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues-Reference-Cited by-同舟云学术

Aluminum Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues

Published:2016-09-14 Issue:29 Volume:2016 Page:5037-5044
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Kotek Vladislav¹,Polák Peter¹,Dvořáková Hana²,Tobrman Tomáš¹^ORCID

Affiliation:

1. Department of Organic Chemistry; University of Chemistry and Technology, Prague; Technická 5 16628 Prague 6 Czech Republic

2. Laboratory of NMR Spectroscopy; University of Chemistry and Technology, Prague; Technická 5 16628 Prague 6 Czech Republic

Funder

MSMT

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference80 articles.

1. Four- and Sixfold Tandem-Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches

2. Vier- und sechsfache Tandem-Dominoreaktionen zur Synthese von dimeren tetrasubstituierten Alkenen als molekulare Doppelschalter

3. Photoredox‐Catalyzed Stereoselective Conversion of Alkynes into Tetrasubstituted Trifluoromethylated Alkenes

4. Photoredox-Catalyzed Stereoselective Conversion of Alkynes into Tetrasubstituted Trifluoromethylated Alkenes

5. A detachable ester bond enables perfect Z-alkylations of olefins for the synthesis of tri- and tetrasubstituted alkenes

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