August 4, 2011Angewandte Chemie

Highly Enantioselective Synthesis of Axially Chiral Biarylphosphonates: Asymmetric Suzuki–Miyaura Coupling Using High‐Molecular‐Weight, Helically Chiral Polyquinoxaline‐Based Phosphines

View Full Paper

Ask AI

Bookmark

Abstract

Katalytische Spirale: In Gegenwart helical-chiraler Polychinoxalin-basierter Phosphane (PQXphos) mit hohem Molekulargewicht gelingen hoch enantioselektive Suzuki-Miyaura-Kupplungen von 1-Brom-2-naphthalinphosphonsäureestern mit o-Methylphenylboronsäuren.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Yamamoto et al. (2011) studied this question.

synapsesocial.com/papers/6a898398439f8b7e01432bae https://doi.org/10.1002/ange.201103792

View Full Paper

Ask AI

Bookmark

Highly Enantioselective Synthesis of Axially Chiral Biarylphosphonates: Asymmetric Suzuki–Miyaura Coupling Using High‐Molecular‐Weight, Helically Chiral Polyquinoxaline‐Based Phosphines

Abstract

Discussion

Cite This Study

Highly Enantioselective Synthesis of Axially Chiral Biarylphosphonates: Asymmetric Suzuki–Miyaura Coupling Using High‐Molecular‐Weight, Helically Chiral Polyquinoxaline‐Based Phosphines

Abstract

Discussion

Cite This Study

Also Consider

Also Consider