2006
DOI: 10.1016/j.jorganchem.2006.03.024
|View full text |Cite
|
Sign up to set email alerts
|

Asymmetric synthesis of a P-chiral heteroditopic ligand via chiral metal template promoted cycloaddition between 3,4-dimethyl-1-phenylphosphole and its sulfonated analog

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2007
2007
2020
2020

Publication Types

Select...
6
1

Relationship

3
4

Authors

Journals

citations
Cited by 16 publications
(2 citation statements)
references
References 36 publications
0
2
0
Order By: Relevance
“…One might also note that an example of a complex with an S-donor trans to C was also found for a polycyclic P^P]S variant of 1. [19] Thus, as observed in earlier arguments regarding hard-soft effects, sometimes the opposite donor is preferred and the selectivity is antisymbiotic. This suggests that some revision of the "rule of thumb for isomeric preferences" is in order.…”
Section: (K 2 -Dman-cn)pd(dppme)mentioning
confidence: 62%
“…One might also note that an example of a complex with an S-donor trans to C was also found for a polycyclic P^P]S variant of 1. [19] Thus, as observed in earlier arguments regarding hard-soft effects, sometimes the opposite donor is preferred and the selectivity is antisymbiotic. This suggests that some revision of the "rule of thumb for isomeric preferences" is in order.…”
Section: (K 2 -Dman-cn)pd(dppme)mentioning
confidence: 62%
“…By using bulky chiral cyclo-metalated compounds, some asymmetric Diels-Alder reactions proceed at the metal [84][85][86][87][88]. For example, the organopalladium complex containing the (S)-form of ortho-palladated (1-(dimethylamino)ethyl)-naphthalene has been used successfully as a chiral template to promote asymmetric cyclo-addition reactions between coordinated 3,4-dimethyl-1-phenylphosphole 27-1 and a dienophile (N,N-dimethy lacrylamide or styrene) via an endo pathway, that proceed to give the compound 27-2 as shown in Eq.…”
Section: Diels-alder Reactions and Other Reactionsmentioning
confidence: 99%