-
7
-
-
77954653022
-
-
For recent reviews on phosphonic acids and their derivatives as inhibitors:
-
C. A. Ramsden Science of Synthesis 2007 31 2035
-
(2007)
Science of Synthesis
, vol.31
, pp. 2035
-
-
Ramsden, C.A.1
-
39
-
-
35548969911
-
-
Recent advance in catalytic asymmetric synthesis of a-hydroxy or amino allyl phosphonates:
-
A. A. Fokin A. G. Yurchenko V. N. Rodionov P. A. Gunchenko R. I. Yurchenko A. Reichenberg J. Wiesner M. Hintz H. Jomaa P. R. Schreiner Org. Lett. 2007 9 4379
-
(2007)
Org. Lett.
, vol.9
, pp. 4379
-
-
Fokin, A.A.1
Yurchenko, A.G.2
Rodionov, V.N.3
Gunchenko, P.A.4
Yurchenko, R.I.5
Reichenberg, A.6
Wiesner, J.7
Hintz, M.8
Jomaa, H.9
Schreiner, P.R.10
-
41
-
-
38049080542
-
-
X. Zhou X. Liu X. Yang D. Shang J. Xin X. Feng Angew. Chem., Int. Ed. 2008 47 392
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 392
-
-
Zhou, X.1
Liu, X.2
Yang, X.3
Shang, D.4
Xin, J.5
Feng, X.6
-
44
-
-
74849104656
-
-
Allylphosphonates have been widely used in the preparation of dienes and polyenes, an advantage of allylphosphonates in the olefination over the corresponding phosphonium salts is exemplified by their stereoselectivity and stereospecificity observed in the reactions:
-
K. Suyama Y. Sakai K. Matsumoto B. Saito T. Katsuki Angew. Chem., Int. Ed. 2010 49 797
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 797
-
-
Suyama, K.1
Sakai, Y.2
Matsumoto, K.3
Saito, B.4
Katsuki, T.5
-
51
-
-
0005934392
-
-
Wiley, New York, 73
-
For selected publications on the Horner-Wadsworth-Emmons reaction: W. S. Wadsworth, Jr, Organic Reactions, Wiley, New York, 1977, Vol. 25, pp 73
-
(1977)
Organic Reactions
, vol.25
-
-
Wadsworth Jr., W.S.1
-
52
-
-
0003942864
-
-
Wiley, New York, Chapter 14 Recent advance in stereoselective allylphosphonate (phosphono unsaturated esters) synthesis employing Baylis-Hillman adducts:
-
E. L. Eliel, and S. H. Wilen, Stereochemistry of Organic Compounds, Wiley, New York, 1994, Chapter 14
-
(1994)
Stereochemistry of Organic Compounds
-
-
Eliel, E.L.1
Wilen, S.H.2
-
58
-
-
34548524770
-
-
Typical condition: BSA, substrate, dialkylphosphite in 1:1:1 ratio, heated for reflux for 2-4 days in THF. The in situ formation of silyl phosphonates was often envisaged as a key to enhance the nucleophilicity of the dialkylphosphites, however, the Lewis acidic nature of silylating reagent may also enhance the electrophilicity of carbonyls towards nucleophilic addition, especially at higher temperature for the effect of protic acid on alkylphosphonylation with conjugated imine:
-
P. A. Badkar N. P. Rath C. D. Spilling Org. Lett. 2007 9 3619
-
(2007)
Org. Lett.
, vol.9
, pp. 3619
-
-
Badkar, P.A.1
Rath, N.P.2
Spilling, C.D.3
-
61
-
-
0346956243
-
-
Although it received much less attention, we found that acrylonitrile derived Baylis-Hillman adducts also undergo phosphonylation, providing the corresponding dialkyl phosphonates with an electronically activated E-allyl dialkylphosphonates, see ref. 16c Metathesis strategy:
-
D. J. Martin M. Gordon C. E. Griffin Tetrahedron 1967 23 1831
-
(1967)
Tetrahedron
, vol.23
, pp. 1831
-
-
Martin, D.J.1
Gordon, M.2
Griffin, C.E.3
-
72
-
-
77954642597
-
-
Wiley-Interscience, New York, Part 1
-
G. A. Olah, Aromatic allylation and Related Reactions, Wiley-Interscience, New York, 1964, Vol. 2, Part 1
-
(1964)
Aromatic Allylation and Related Reactions
, vol.2
-
-
Olah, G.A.1
-
73
-
-
71949116045
-
Friedel-Crafts Alkylation Chemistry
-
Marcel Dekker, New York
-
R. M. Roberts, and A. A. Khalaf, Friedel-Crafts Alkylation Chemistry. A Century of Discovery, Marcel Dekker, New York, 1984
-
(1984)
A Century of Discovery
-
-
Roberts, R.M.1
Khalaf, A.A.2
-
74
-
-
0001586671
-
Friedel-Crafts Alkylations in
-
B. M. Trost, I. Flemin, Pergamon Press, Oxford
-
G. A. Olah, R. Krishnamurti, G. K. S. Prakash, Friedel-Crafts Alkylations in Comprehensive Organic Synthesis, ed., B. M. Trost,,, I. Flemin,, Pergamon Press, Oxford, 1991
-
(1991)
Comprehensive Organic Synthesis, Ed.
-
-
Olah, G.A.1
Krishnamurti, R.2
Prakash, G.K.S.3
-
83
-
-
38349062995
-
-
Pioneer work on highly regio- and stereoselective aromatic allylation of allylic alcohols mediated by iron carbonyl:
-
E. Ramesh R. Raghunathan Tetrahedron Lett. 2008 49 1125
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1125
-
-
Ramesh, E.1
Raghunathan, R.2
-
87
-
-
45449100756
-
-
Some potential applications for the aromatic allylation products:
-
W. Rao P. W. H. Chan Org. Biomol. Chem. 2008 6 2426
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 2426
-
-
Rao, W.1
Chan, P.W.H.2
-
90
-
-
33748059638
-
-
Mechanism of the hydrolysis of condensed phosphates in aqueous organic solvents:
-
E. N. Walsh J. Am. Chem. Soc. 1959 81 3023
-
(1959)
J. Am. Chem. Soc.
, vol.81
, pp. 3023
-
-
Walsh, E.N.1
-
94
-
-
35548986297
-
-
J. J. Li, E. J. Corey, John Wiley & Sons
-
A. R. E. Brewer, in Name Reactions for Functional Group Transformations, ed., J. J. Li,,, E. J. Corey,, John Wiley & Sons, 2007
-
(2007)
Name Reactions for Functional Group Transformations, Ed.
-
-
Brewer In, A.R.E.1
-
96
-
-
0025934002
-
Structural requirements for the inhibition of human monocyte carboxylesterase by organophosphorus
-
A. M. Saboori D. M. Lang D. S. Newcombe Structural requirements for the inhibition of human monocyte carboxylesterase by organophosphorus Chem.-Biol. Interact. 1991 80 327
-
(1991)
Chem.-Biol. Interact.
, vol.80
, pp. 327
-
-
Saboori, A.M.1
Lang, D.M.2
Newcombe, D.S.3
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