Chemoselective Suzuki-Miyaura reactions of 4-bromo-3- O -triflyl-estrone. Synthesis and atropisomerism of arylated estrones-Reference-Cited by-同舟云学术

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Chemoselective Suzuki-Miyaura reactions of 4-bromo-3- O -triflyl-estrone. Synthesis and atropisomerism of arylated estrones

Published:2018-06 Issue:23 Volume:74 Page:2825-2836
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Jopp Stefan,Wallaschkowski Tina,Ehlers Peter,Frank Eva,Schneider Gyula,Wölfling János,Mernyák Erzsébet,Villinger Alexander,Langer Peter

Funder

BMBF

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. P. L. Yeagle Biochimie 1991, 73, 1303–1310.

2. Human Anatomy and Physiology;Hoehn,2010

3. H. Kuhl Climacteric 2005, 8, 3–63.

4. Hormone und Hormonsystem 3;Kleine,2014

5. Preparation of 16-formylestradiol and the 16-(α-methylenebutanolide) derivative

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1. Structure‐Activity Relationships of Glucose‐based Pd^II‐Bis(NHC) Complexes in a Model Suzuki‐Miyaura Reaction;European Journal of Organic Chemistry;2024-05-22

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3. ortho-Heterobimetallic Arylene Complex: A New Platform for Regioselective Difunctionalization;Synlett;2023-05-03

4. Recent advances in the application of ligands in palladium-catalyzed chemoselective coupling reactions at C–Br, C–OTf, and C–Cl sites;Organic Chemistry Frontiers;2023

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