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0003594801
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Mulzer, J.; Altenbach, H.-J.; Braun, M.; Krohn, K.; Reissig, H.-U. Organic Synthesis Highlights; VCH: Weinheim, 1991.
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Mulzer, J.1
Altenbach, H.-J.2
Braun, M.3
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14
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0020169638
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Prelog, V.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1982, 21, 567.
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Prelog, V.1
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20
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0001083790
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Fujita, S. Tetrahedron 1990, 46, 5943-5954.
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Tetrahedron
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Fujita, S.1
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24
-
-
85033850585
-
-
For the re/si-nomenclature, see ref 8
-
For the re/si-nomenclature, see ref 8.
-
-
-
-
25
-
-
1842474029
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Fagan, P. J.; Calarese, J. C.; Malone, B. J. Am. Chem. Soc. 1991, 113, 9408-9409.
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33748895937
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Hirsch, A.; Lamparth, I.; Karfunkel, H. R. Angew. Chem., Int. Ed. Engl. 1994, 33, 437-438.
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Hirsch, A.1
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Karfunkel, H.R.3
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30
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33748888245
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-
Henderson, C. C; Rohifang, C. M.; Assink, R. A.; Cahill, P. A. Angew. Chem., Int. Ed. Engl. 1994, 33, 786-788.
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Henderson, C.C.1
Rohifang, C.M.2
Assink, R.A.3
Cahill, P.A.4
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31
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0028765756
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Hirsch, A.; Lamparth, I.; Gösser, T.; Karfunkel, H. R. J. Am. Chem. Soc. 1994, 116, 9385-9386.
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Hirsch, A.1
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32
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85002102057
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36
-
-
85033852602
-
-
note
-
Table 1 of ref 35 contains misprints. Edges [6:6] of 1 should be corrected to be edges [5:6] and edges [5:6] of 1 should be corrected to be edges [6:6]. The [6:6] edges in the right column of page 3216 and the [5:6] edges in the left column of page 3217 should be corrected into [5:6] edges and [6:6] edges, respectively.
-
-
-
-
38
-
-
0000300919
-
-
3 column should be corrected into zero. However, the total value 832592 remains unaffected and correct, since we have 830212 + 2380 = 832592.
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(1990)
Bull. Chem. Soc. Jpn.
, vol.63
, pp. 2759-2769
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Fujita, S.1
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39
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51649146515
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Pólya, G. Acta Math. 1937, 68, 145-254.
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Acta Math.
, vol.68
, pp. 145-254
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Pólya, G.1
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41
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0001296536
-
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For reviews on chemical applications of the Pólya-Redfield theorem, see: Rouvray, D. H. Chem. Soc. Rev. 1974, 3, 355. Chemical Applications of Graph Theory; Balaban, A. T. Ed.; Academic: London, 1976. Balasubramanian, K. Chem. Rev. 1985, 85, 599.
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Rouvray, D.H.1
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42
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0001296536
-
-
Academic: London
-
For reviews on chemical applications of the Pólya-Redfield theorem, see: Rouvray, D. H. Chem. Soc. Rev. 1974, 3, 355. Chemical Applications of Graph Theory; Balaban, A. T. Ed.; Academic: London, 1976. Balasubramanian, K. Chem. Rev. 1985, 85, 599.
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(1976)
Chemical Applications of Graph Theory
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Balaban, A.T.1
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43
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0000134810
-
-
For reviews on chemical applications of the Pólya-Redfield theorem, see: Rouvray, D. H. Chem. Soc. Rev. 1974, 3, 355. Chemical Applications of Graph Theory; Balaban, A. T. Ed.; Academic: London, 1976. Balasubramanian, K. Chem. Rev. 1985, 85, 599.
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Chem. Rev.
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Balasubramanian, K.1
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45
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0000907123
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Balasubramanian, K. J. Phys. Chem. 1993, 97, 6990-6998; Chem. Phys. Lett. 1995, 237, 229-238.
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Balasubramanian, K.1
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46
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0002176580
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Balasubramanian, K. J. Phys. Chem. 1993, 97, 6990-6998; Chem. Phys. Lett. 1995, 237, 229-238.
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-
-
56
-
-
85033844781
-
-
note
-
A proligand pair can be regarded as a proligand in an abstract fashion. From this standpoint, such a proligand is reversely considered to have an inner structure. This is an alternative way to treat higher relationships.
-
-
-
-
57
-
-
85033855638
-
-
note
-
A proligand pair (bond pair) is considered to be composed of two proligands selected from S, T, P, and P, where S and T are achiral proligands, and P and P are chiral proligands with inverse chirality. Then, we have three types of achiral segments, S-S, S-T, and P-P, which correspond to the terms equilocative, dialocative and mesolocative, respectively.
-
-
-
-
58
-
-
0001288744
-
-
Hawkins, J. M.; Meyer, A.; Lewis, T. A.; Bunz, U.; Nunlist, R.; Ball, G. E.; Ebbesen, T. W.; Tanigaki, K. J. Am. Chem. Soc. 1992, 114, 7954-7955.
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J. Am. Chem. Soc.
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Hawkins, J.M.1
Meyer, A.2
Lewis, T.A.3
Bunz, U.4
Nunlist, R.5
Ball, G.E.6
Ebbesen, T.W.7
Tanigaki, K.8
-
59
-
-
85033833109
-
-
note
-
l)-orbit in 16. Although the locativity terms are convenient to communicate stereochemical relationships, elaborate consideration should be based on the sphericity concept to avoid undesired confusion.
-
-
-
-
60
-
-
85033850958
-
-
note
-
s)-orbits. Since they are energetically different from each other, the decarboxylation is a chemoselective achiral process.
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-
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