-
3
-
-
0001427691
-
-
This name is based on the nomenclature suggested by
-
This name is based on the nomenclature suggested by R. Huisgen, Angew. Chem., 75, 604 (1963).
-
(1963)
Angew. Chem.
, vol.75
, pp. 604
-
-
Huisgen, R.1
-
5
-
-
33144470975
-
-
See, for a theoretical discussion of the situation in thiophene
-
See, for a theoretical discussion of the situation in thiophene, M. J. Bielefeld and D. D. Fitts, Chern. Soc., 88, 4804 (1966).
-
(1966)
Chern. Soc.
, vol.88
, pp. 4804
-
-
Bielefeld, M.J.1
Fitts, D.D.2
-
6
-
-
2942699798
-
-
C. C. Price, J. Follweiler, N. Pirelahi, and M. Siskin, J. Org. Chern., 36, 791 (1971);
-
(1971)
J. Org. Chern.
, vol.36
, pp. 791
-
-
Price, C.C.1
Follweiler, J.2
Pirelahi, N.3
Siskin, M.4
-
7
-
-
0003102351
-
-
C. C. Price, M. Siskin, and C. K. Miao, J. Org. Chern., 36, 794 (1971);
-
(1971)
J. Org. Chern.
, vol.36
, pp. 794
-
-
Price, C.C.1
Siskin, M.2
Miao, C.K.3
-
9
-
-
49949132781
-
-
See, for example, (a)
-
See, for example, (a) J. Strating, L. Thijs, and B. Zwanenburg, Tetrahedron Lett., 65 (1966);
-
(1966)
Tetrahedron Lett.
, pp. 65
-
-
Strating, J.1
Thijs, L.2
Zwanenburg, B.3
-
10
-
-
84982069995
-
-
B. Zwanenburg, L. Thijs, and J. Strating, Recl. Trav. Chim. Pays-Bas, 86, 577 (1967);
-
(1967)
Recl. Trav. Chim. Pays-Bas
, vol.86
, pp. 577
-
-
Zwanenburg, B.1
Thijs, L.2
Strating, J.3
-
15
-
-
85022409566
-
-
G. Nickless, Ed., Elsevier, New York, N. Y.
-
H. G. Heal, “Inorganic Sulfur Chemistry,” G. Nickless, Ed., Elsevier, New York, N. Y., 1968, p 459.
-
(1968)
Inorganic Sulfur Chemistry
, pp. 459
-
-
Heal, H.G.1
-
16
-
-
0041192679
-
-
For a 1,3-dipolar addition of 7, see
-
For a 1,3-dipolar addition of 7, see M. R. Brinkman and C. W. Allen, J. Amer. Chem. Soc., 94, 1550 (1972).
-
(1972)
J. Amer. Chem. Soc.
, vol.94
, pp. 1550
-
-
Brinkman, M.R.1
Allen, C.W.2
-
20
-
-
0009298978
-
-
and references contained therein
-
G. Kresze and W. Wucherpfennig, Angew. Chem., 79, 109 (1967), and references contained therein.
-
(1967)
Angew. Chem.
, vol.79
, pp. 109
-
-
Kresze, G.1
Wucherpfennig, W.2
-
21
-
-
0004009372
-
-
For a description, see Interscience, New York, N. Y.
-
For a description, see F. A. Cotton and E. Wilkinson, “Advanced Inorganic Chemistry,” Interscience, New York, N. Y., 1966, pp 534-540.
-
(1966)
Advanced Inorganic Chemistry
, pp. 534-540
-
-
Cotton, F.A.1
Wilkinson, E.2
-
22
-
-
33748968666
-
-
For early studies on the addition of sulfur dioxide to dienes, see
-
For early studies on the addition of sulfur dioxide to dienes, see H. J. Backer, J. Strating, and C. M. H. Kool, Recl. Trav. Chim. Pays-Bas, 58, 778 (1939).
-
(1939)
Recl. Trav. Chim. Pays-Bas
, vol.58
, pp. 778
-
-
Backer, H.J.1
Strating, J.2
Kool, C.M.H.3
-
23
-
-
0003117406
-
-
For an early MO description, see (a)
-
For an early MO description, see (a) H. P. Koch and W. E. Moffit, Trans. Faraday Soc., 47, 7 (1951);
-
(1951)
Trans. Faraday Soc.
, vol.47
, pp. 7
-
-
Koch, H.P.1
Moffit, W.E.2
-
24
-
-
0003438540
-
-
also Cornell University Press, 3rd ed, Ithaca, N. Y.
-
also L. Pauling, “The Nature of the Chemical Bond,” Cornell University Press, 3rd ed, Ithaca, N. Y., 1960.
-
(1960)
The Nature of the Chemical Bond
-
-
Pauling, L.1
-
27
-
-
0000430914
-
-
R. Huisgen, W. Scheer, and H. Huber, J. Amer. Chem. Soc., 89, 1753 (1967);
-
(1967)
J. Amer. Chem. Soc.
, vol.89
, pp. 1753
-
-
Huisgen, R.1
Scheer, W.2
Huber, H.3
-
28
-
-
84981766677
-
-
R. Huisgen, W. Scheer, and H. Mäder, Angew. Chem. Int. Ed. Engl, 8, 602 (1969);
-
(1969)
Angew. Chem. Int. Ed. Engl
, vol.8
, pp. 602
-
-
Huisgen, R.1
Scheer, W.2
Mäder, H.3
-
29
-
-
84981799638
-
-
R. Huisgen, W. Scheer, H. Mäder, and K. Brunn, Angew. Chem. Int. Ed. Engl, 8, 604 (1969);
-
(1969)
Angew. Chem. Int. Ed. Engl
, vol.8
, pp. 604
-
-
Huisgen, R.1
Scheer, W.2
Mäder, H.3
Brunn, K.4
-
33
-
-
37049128862
-
-
J. H. Hall, R. Huisgen, C. H. Ross, and W. Scheer, Chem. Commun., 1188 (1971).
-
(1971)
Chem. Commun.
, pp. 1188
-
-
Hall, J.H.1
Huisgen, R.2
Ross, C.H.3
Scheer, W.4
-
39
-
-
0344887785
-
-
T. Do-Minh, A. M. Trozzolo, and G. W. Griffin, J. Amer. Chem. Soc., 92, 1402 (1970);
-
(1970)
J. Amer. Chem. Soc.
, vol.92
, pp. 1402
-
-
Do-Minh, T.1
Trozzolo, A.M.2
Griffin, G.W.3
-
43
-
-
37049126415
-
-
A. Dahmen, H. Hamberger, R. Huisgen, and V. Markowsky, Chem. Commun., 1192 (1971).
-
(1971)
Chem. Commun.
, pp. 1192
-
-
Dahmen, A.1
Hamberger, H.2
Huisgen, R.3
Markowsky, V.4
-
46
-
-
37049119308
-
-
The principle of olefin synthesis by a “twofold extrusion process” has been elegantly enunciated by
-
The principle of olefin synthesis by a “twofold extrusion process” has been elegantly enunciated by D. H. R. Barton and B. J. Willis, J. Chem. Soc., Perkin Trans. I, 305 (1972);
-
(1972)
J. Chem. Soc., Perkin Trans. I
, pp. 305
-
-
Barton, D.H.R.1
Willis, B.J.2
-
47
-
-
85022623777
-
-
Among the compounds investigated was a thiadiazolidine (see further) that was concurrently prepared by our group.1 We are grateful to Professor Barton for correspondence on this matter
-
Chem. Commun., 1225 (1970), Among the compounds investigated was a thiadiazolidine (see further) that was concurrently prepared by our group.1 We are grateful to Professor Barton for correspondence on this matter.
-
(1970)
Chem. Commun.
, pp. 1225
-
-
-
48
-
-
0001833189
-
-
See, for an early example
-
See, for an early example, E. B. Knott, J. Chem. Soc., 916 (1955).
-
(1955)
J. Chem. Soc.
, pp. 916
-
-
Knott, E.B.1
-
50
-
-
84982071103
-
-
G. Wittig, E. Knaus, and K. Niethammer, Justus Liebigs Ann. Chem., 630, 10 (1960).
-
(1960)
Justus Liebigs Ann. Chem.
, vol.630
, pp. 10
-
-
Wittig, G.1
Knaus, E.2
Niethammer, K.3
-
51
-
-
0038865247
-
-
R. Mayer, H. Kleinert, S. Richter, and K. Gewald, Angew. Chem., 74, 118 (1962).
-
(1962)
Angew. Chem.
, vol.74
, pp. 118
-
-
Mayer, R.1
Kleinert, H.2
Richter, S.3
Gewald, K.4
-
52
-
-
33947300585
-
-
See, for example, (a)
-
See, for example, (a) M. P. Cava and G. E. M. Husbands, J. Amer. Chem. Soc., 91, 3952 (1969);
-
(1969)
J. Amer. Chem. Soc.
, vol.91
, pp. 3952
-
-
Cava, M.P.1
Husbands, G.E.M.2
-
56
-
-
0042121885
-
-
R. S. Becker, R. O. Bost, J. Kolc, N. R. Bertonière, R. L. Smith, and G. W. Griffin, J. Amer. Chem, Soc., 92, 1302 (1970).
-
(1970)
J. Amer. Chem, Soc.
, vol.92
, pp. 1302
-
-
Becker, R.S.1
Bost, R.O.2
Kolc, J.3
Bertonière, N.R.4
Smith, R.L.5
Griffin, G.W.6
-
61
-
-
84982062155
-
-
H. H. Inhoffen, R. Jonas, H. Kroesche, and U. Eder, Justus Liebigs Ann. Chem., 694, 19 (1966).
-
(1966)
Justus Liebigs Ann. Chem.
, vol.694
, pp. 19
-
-
Inhoffen, H.H.1
Jonas, R.2
Kroesche, H.3
Eder, U.4
-
62
-
-
0001313088
-
-
G. M. Kaufman, J. A. Smith, G. G. Vander Stouw, and H. Shechter, J. Amer. Chem. Soc., 87, 935 (1965).
-
(1965)
J. Amer. Chem. Soc.
, vol.87
, pp. 935
-
-
Kaufman, G.M.1
Smith, J.A.2
Vander Stouw, G.G.3
Shechter, H.4
-
63
-
-
0001784199
-
-
M. J. Janssen, Ed., Interscience, New York, N. Y.
-
R. Mayer, “Organosulfur Chemistry,” M. J. Janssen, Ed., Interscience, New York, N. Y., 1967, pp 219-240.
-
(1967)
Organosulfur Chemistry
, pp. 219-240
-
-
Mayer, R.1
-
64
-
-
33947290999
-
-
reported the successful isolation of 1,3,4-thiadiazolines from the reactions of diazomethane with some spiro thioketones
-
A. P. Krapcho, D. R. Raa, M. P. silvon, and B. Abegaz, J. Org. Chem., 36, 3885 (1971), reported the successful isolation of 1,3,4-thiadiazolines from the reactions of diazomethane with some spiro thioketones.
-
(1971)
J. Org. Chem.
, vol.36
, pp. 3885
-
-
Krapcho, A.P.1
Raa, D.R.2
silvon, M.P.3
Abegaz, B.4
-
67
-
-
85050328347
-
-
F. Yoneda, K. Suzuki, and Y. Nitta, J. Amer. Chem. Soc., 88, 2328 (1966).
-
(1966)
J. Amer. Chem. Soc.
, vol.88
, pp. 2328
-
-
Yoneda, F.1
Suzuki, K.2
Nitta, Y.3
-
70
-
-
0006938942
-
-
E. L. Eliel, M. H. Gianni, T. H. Williams, and J. D. Stothers, Tetrahedron Lett., 741 (1962).
-
(1962)
Tetrahedron Lett.
, pp. 741
-
-
Eliel, E.L.1
Gianni, M.H.2
Williams, T.H.3
Stothers, J.D.4
-
80
-
-
6444239161
-
-
F. G. Bordwell, N. M. Andersen, and B. M. Pitt, J. Amer. Chem. Soc., 76, 1082 (1959).
-
(1959)
J. Amer. Chem. Soc.
, vol.76
, pp. 1082
-
-
Bordwell, F.G.1
Andersen, N.M.2
Pitt, B.M.3
-
81
-
-
0003466385
-
-
Pergamon Press, Oxford
-
J. W. Emsley, J. Feeney, and L. H. Sutcliffe, “High Resolution Nuclear Magnetic Resonance,” Vol. 2, Pergamon Press, Oxford, 1966, p 703;
-
(1966)
High Resolution Nuclear Magnetic Resonance
, vol.2
, pp. 703
-
-
Emsley, J.W.1
Feeney, J.2
Sutcliffe, L.H.3
-
83
-
-
0012180729
-
-
R. J. Crawford, A. Mishra, and R. J. Dummel, J. Amer. Chem. Soc., 88, 3959 (1906).
-
(1906)
J. Amer. Chem. Soc.
, vol.88
, pp. 3959
-
-
Crawford, R.J.1
Mishra, A.2
Dummel, R.J.3
-
84
-
-
0003971643
-
-
McGraw-Hill, New York, N. Y.
-
E. L. Eliel, “The Stereochemistry of Carbon Compounds,” McGraw-Hill, New York, N. Y., 1962, pp 248-252.
-
(1962)
The Stereochemistry of Carbon Compounds
, pp. 248-252
-
-
Eliel, E.L.1
-
89
-
-
33947299307
-
-
A “recoil” effect resulting in inversion of configuration at the carbon atom is suggested to be operative at least in bicyclic compounds
-
A “recoil” effect resulting in inversion of configuration at the carbon atom is suggested to be operative at least in bicyclic compounds: E. L. Allred and R. L. Smith, J. Amer. Chem. Soc., 91, 6766 (1969).
-
(1969)
J. Amer. Chem. Soc.
, vol.91
, pp. 6766
-
-
Allred, E.L.1
Smith, R.L.2
-
90
-
-
0001387888
-
-
Strong conformational preferences in the transition states for decomposition of diazabicyclo-[2.1.0]pentane derivatives has been demonstrated by
-
Strong conformational preferences in the transition states for decomposition of diazabicyclo-[2.1.0]pentane derivatives has been demonstrated by J. A. Berson and S. S. Olin, J. Amer. Chem. Soc., 91, 777 (1969).
-
(1969)
J. Amer. Chem. Soc.
, vol.91
, pp. 777
-
-
Berson, J.A.1
Olin, S.S.2
-
91
-
-
37049163420
-
-
That thiocarbonyl ylides should be nonlinear follows directly from application of Walsh's rules: (a) 2288, 2296, 2301
-
That thiocarbonyl ylides should be nonlinear follows directly from application of Walsh's rules: (a) A. D. Walsh, J. Chem. Soc., 2260, 2266, 2288, 2296, 2301 (1953);
-
(1953)
J. Chem. Soc.
, vol.2260
, pp. 2266
-
-
Walsh, A.D.1
-
92
-
-
33947290373
-
-
Y. Takahata, G. W. Schnuelle, and R. G. Parr, J. Amer. Chem. Soc., 93, 784 (1971);
-
(1971)
J. Amer. Chem. Soc.
, vol.93
, pp. 784
-
-
Takahata, Y.1
Schnuelle, G.W.2
Parr, R.G.3
-
94
-
-
85022716460
-
-
For a general review of the geometry of sulfur compounds, see
-
For a general review of the geometry of sulfur compounds, see S. C. Abrahams, Quart. Rev., X, 407 (1956).
-
(1956)
Quart. Rev., X
, pp. 407
-
-
Abrahams, S.C.1
-
99
-
-
84981760247
-
-
R. Criegee, E. Vogel, and H. Höger, Chem. Ber., 85, 144 (1952),
-
(1952)
Chem. Ber.
, vol.85
, pp. 144
-
-
Criegee, R.1
Vogel, E.2
Höger, H.3
-
100
-
-
33947471134
-
-
S. D. Koch, R. M. Kliss, D. V. Lopiekes, and R. J. Wineman, J. Org. Chem., 26, 3122 (1961),
-
(1961)
J. Org. Chem.
, vol.26
, pp. 3122
-
-
Koch, S.D.1
Kliss, R.M.2
Lopiekes, D.V.3
Wineman, R.J.4
-
101
-
-
0003514816
-
-
Wiley, New York, N. Y.
-
L. F. Fieser and M. Fieser, “Reagents for Organic Synthesis,” Wiley, New York, N. Y., p 136.
-
Reagents for Organic Synthesis
, pp. 136
-
-
Fieser, L.F.1
Fieser, M.2
-
102
-
-
0000530877
-
-
H. R. Snyder, J. M. Stewart, and J. B. Ziegler, J. Amer. Chem. Soc., 69, 2672 (1947).
-
(1947)
J. Amer. Chem. Soc.
, vol.69
, pp. 2672
-
-
Snyder, H.R.1
Stewart, J.M.2
Ziegler, J.B.3
-
103
-
-
0000755143
-
-
A. R. Bader, R. P. Buckley, F. Leavitt, and M. Szwarc, J. Amer. Chem. Soc., 79, 5621 (1957).
-
(1957)
J. Amer. Chem. Soc.
, vol.79
, pp. 5621
-
-
Bader, A.R.1
Buckley, R.P.2
Leavitt, F.3
Szwarc, M.4
-
104
-
-
85027474296
-
-
See, for example
-
See, for example, P. Natalis and J. F. Franklin, Bull. Soc. Chim. Belg., 75, 328 (1966).
-
(1966)
Bull. Soc. Chim. Belg.
, vol.75
, pp. 328
-
-
Natalis, P.1
Franklin, J.F.2
-
105
-
-
33644840918
-
-
the reason for the discrepancy in melting point is unknown
-
M. A. Youtz and P. P. Perkins, J. Amer. Chem. Soc., 51, 3508 (1929); the reason for the discrepancy in melting point is unknown.
-
(1929)
J. Amer. Chem. Soc.
, vol.51
, pp. 3508
-
-
Youtz, M.A.1
Perkins, P.P.2
|