Sterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi‐Purpose Asymmetric Organocatalysts-Reference-Cited by-同舟云学术

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Sterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi‐Purpose Asymmetric Organocatalysts

Published:2022-04-26 Issue:26 Volume:134 Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Scharinger Fabian¹^ORCID,Pálvölgyi Ádám Márk¹^ORCID,Weisz Melanie¹,Weil Matthias²^ORCID,Stanetty Christian¹^ORCID,Schnürch Michael¹^ORCID,Bica‐Schröder Katharina¹^ORCID

Affiliation:

1. Institute of Applied Synthetic Chemistry, TU Wien Getreidemarkt 9/163 1060 Wien Austria

2. Institute of Chemical Technologies and Analytics, TU Wien Getreidemarkt 9/163 1060 Wien Austria

Funder

Austrian Science Fund

H2020 European Research Council

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202202189

Reference65 articles.

1. Asymmetric organocatalysis

2. Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles

3. Asymmetric synthesis of warfarin and its analogs catalyzed by C2-symmetric squaramide-based primary diamines

4. Camphor-derived C1-symmetric chiral diamine organocatalysts for asymmetric Michael addition of nitroalkanes to enones

5. Organocatalytic Asymmetric β-Hydroxylation of α,β-Unsaturated Ketones

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