Stereoselective Domino Heck‐Suzuki Reactions-Reference-Cited by-同舟云学术

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Stereoselective Domino Heck‐Suzuki Reactions

Published:2022-12-30 Issue:3 Volume:26 Page:
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur J Org Chem

Author:

Braun Manfred¹^ORCID

Affiliation:

1. Institute of Organic and Macromolecular Chemistry Heinrich-Heine-University Düsseldorf Universitätsstr. 1 40225 Düsseldorf Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202201282

Reference107 articles.

1.

2. L.-F. Tietze G. Brasche K. M. Gericke Domino Reactions in Organic Synthesis Wiley-VCH: Weinheim Germany2006;

3. L.-F. Tietze (Ed.) Domino Reactions: Concepts for Efficient Organic Synthesis Wiley-VCH Weinheim Germany2014;

4. H. Pellissier Asymmetric Domino Reactions RSC Catalysis Series No. 10 The Royal Society of Chemistry Cambridge2013;

5. Z. J. Witczak R. Bielski (Eds.) Domino and Intramolecular Rearrangement Reactions as Advanced Synthetic Methods in Glycoscience Wiley Hoboken USA2016;

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1. Mizoroki-Heck-type transformations in natural product synthesis: Case studies in carbopalladation and forging all-carbon quaternary stereocenters;Chem Catalysis;2024-04

2. Palladium-Catalyzed Heck/Suzuki Tandem Reaction of (Z)-1-Iodo-1,6-dienes and Organoboronic Acids;Organic Letters;2024-03-07

3. [DABCO-C18]Br: A novel basic surfactant for the synthesis of dihydropyrano[3,2-c]chromenes and 2-aminobenzochromenes under ambient conditions;Journal of Molecular Liquids;2023-12

4. [ZrFe2O4@SiO2–N–(TMSP)–ASP–Pd(0)] Complex: Synthesis, characterizations, and its application as a nanomagnetic catalyst in cross-coupling and click reactions;Journal of Molecular Structure;2023-11

5. Gold‐Catalyzed 1,2‐Dicarbofunctionalization of Alkynes with Organohalides**;Angewandte Chemie International Edition;2023-09-07

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