The hallmark of nucleophilic phosphine catalysis is the initial nucleophilic addition of a
phosphine to an electrophilic starting material, producing a reactive zwitterionic …

Asymmetric phosphine catalysis showcasing remarkable progress over the past two
decades has emerged as a key synthetic platform for the creation of molecular frameworks …

1. INTRODUCTION The carbon− carbon bond forming reactions is one of the most important
reactions in organic chemistry, and therefore has been and remains an important and a …

Nucleophilic phosphine catalysis is a practical and powerful tool for the synthesis of various
heterocyclic compounds with the advantages of environmentally friendly, metal-free, and …

This review discusses the tertiary phosphines possessing various chiral skeletons that have
been used in asymmetric nucleophilic organocatalytic reactions, including annulations of …

In the last few years, the research area of chiral β-aminophosphines capable of promoting a
wide range of diverse organic transformations has attracted more attention. Their derivatives …

Beyond a doubt organocatalysis belongs to the most exciting and innovative chapters of
organic chemistry today. Organocatalysis has emerged not only as a complement to metal …

Chiral phosphines are versatile Lewis basic catalysts that are capable of promoting a wide
range of asymmetric reactions. In particular, recently designed chiral phosphines based on …

This review is focused on the enantioselective synthesis of 3, 4-dihydropyran derivatives,
whose importance as chiral building blocks in the synthesis of bioactive molecules and …

Two tetraphenylethene (TPE)‐functionalized spiropyran (SP) molecules with very similar
structure were designed and synthesized. The two molecules exhibit aggregation‐induced …