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Chelating phosphines with C2 and C3 symmetry

Emilie Brulé 1
Emilie Brulé
, 
Yuxin Pei 1
Yuxin Pei
, 
Fredrik Lake 1
Fredrik Lake
, 
Fredrik Rahm 1
Fredrik Rahm
, 
Christina Moberg 1
Christina Moberg
10.1070/MC2004v014n06ABEH002026
Published 2004-12-17
Communication , Volume 14, Issue 6, 276-277
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Brulé E. et al. Chelating phosphines with C2 and C3 symmetry // Mendeleev Communications. 2004. Vol. 14. No. 6. pp. 276-277.
GOST all authors (up to 50) Copy
Brulé E., Pei Y., Lake F., Rahm F., Moberg C. Chelating phosphines with C2 and C3 symmetry // Mendeleev Communications. 2004. Vol. 14. No. 6. pp. 276-277.
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TY - JOUR
DO - 10.1070/MC2004v014n06ABEH002026
UR - https://mendcomm.colab.ws/publications/10.1070/MC2004v014n06ABEH002026
TI - Chelating phosphines with C2 and C3 symmetry
T2 - Mendeleev Communications
AU - Brulé, Emilie
AU - Pei, Yuxin
AU - Lake, Fredrik
AU - Rahm, Fredrik
AU - Moberg, Christina
PY - 2004
DA - 2004/12/17
PB - Mendeleev Communications
SP - 276-277
IS - 6
VL - 14
ER -
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@article{2004_Brulé,
author = {Emilie Brulé and Yuxin Pei and Fredrik Lake and Fredrik Rahm and Christina Moberg},
title = {Chelating phosphines with C2 and C3 symmetry},
journal = {Mendeleev Communications},
year = {2004},
volume = {14},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2004v014n06ABEH002026},
number = {6},
pages = {276--277},
doi = {10.1070/MC2004v014n06ABEH002026}
}
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Brulé, Emilie, et al. “Chelating phosphines with C2 and C3 symmetry.” Mendeleev Communications, vol. 14, no. 6, Dec. 2004, pp. 276-277. https://mendcomm.colab.ws/publications/10.1070/MC2004v014n06ABEH002026.

Abstract

Amide formation between ring opened aziridines and 2-(diphenylphosphino)benzoic acid provides an easy access to chelating di-and triphosphines with C2 and C3 symmetry.

References

1.
C2 symmetry and asymmetric induction
Whitesell J.K.
Chemical Reviews, 1989
5.
Synthesis of C3 Symmetric, Optically Active Triamidoamine and Protetraazaphosphatrane
Ishihara K., Karumi Y., Kondo S., Yamamoto H.
Journal of Organic Chemistry, 1998
7.
Asymmetric Allylic Alkylation, an Enabling Methodology
Trost B.M.
Journal of Organic Chemistry, 2004