Home / Publications / Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites

Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites

Mudaris Nurgaleevich Dimukhametov 1
Mudaris Nurgaleevich Dimukhametov
,  , 
Rashid Zagitovich Musin 1
Rashid Zagitovich Musin
10.1070/MC2006v016n01ABEH002221
Published 2006-01-31
Communication , Volume 16, Issue 1, 48-50
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Dimukhametov M. N., Mironov V. F., Musin R. Z. Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites // Mendeleev Communications. 2006. Vol. 16. No. 1. pp. 48-50.
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Dimukhametov M. N., Mironov V. F., Musin R. Z. Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites // Mendeleev Communications. 2006. Vol. 16. No. 1. pp. 48-50.
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TY - JOUR
DO - 10.1070/MC2006v016n01ABEH002221
UR - https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002221
TI - Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites
T2 - Mendeleev Communications
AU - Dimukhametov, Mudaris Nurgaleevich
AU - Mironov, Vladimir Fedorovich
AU - Musin, Rashid Zagitovich
PY - 2006
DA - 2006/01/31
PB - Mendeleev Communications
SP - 48-50
IS - 1
VL - 16
ER -
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@article{2006_Dimukhametov,
author = {Mudaris Nurgaleevich Dimukhametov and Vladimir Fedorovich Mironov and Rashid Zagitovich Musin},
title = {Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites},
journal = {Mendeleev Communications},
year = {2006},
volume = {16},
publisher = {Mendeleev Communications},
month = {Jan},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002221},
number = {1},
pages = {48--50},
doi = {10.1070/MC2006v016n01ABEH002221}
}
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Cite this
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Dimukhametov, Mudaris Nurgaleevich, et al. “Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites.” Mendeleev Communications, vol. 16, no. 1, Jan. 2006, pp. 48-50. https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002221.

Abstract

Iminophosphites, which are formed in the reactions of para-(N-benzylidene)aminophenol with diethyl and ethylene chlorophosphites by the formation of two new intermolecular P–C bonds with the participation of HCl evolved in the course of the reaction, are condensed to form 16-membered P-macrocycles, 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives.

References

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2.
Stereoselective synthesis of 1,4,2‐oxazaphosphorines as precursors of chiral α‐aminophosphonic acids by intramolecular heterocyclization of β‐aldiminoalkylphosphites
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