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2
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85030945857
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Handbook of Chiral Chemicals; Ager, D. J., Ed.; Marcel Dekker: New York, 1999.
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12
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0001374863
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Reviews: (a) Tamaru, Y. J. Organomet. Chem. 1999, 576, 215-231; (b) Montgomery, J. Acc. Chem. Res. 2000, 33, 467-473; (c) Ikeda, S.-i. Acc. Chem. Res. 2000, 33, 511-519; (d) Houpis, I. N.; Lee, J. Tetrahedron 2000, 56, 817-846.
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J. Organomet. Chem.
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Tamaru, Y.1
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0033913798
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Reviews: (a) Tamaru, Y. J. Organomet. Chem. 1999, 576, 215-231; (b) Montgomery, J. Acc. Chem. Res. 2000, 33, 467-473; (c) Ikeda, S.-i. Acc. Chem. Res. 2000, 33, 511-519; (d) Houpis, I. N.; Lee, J. Tetrahedron 2000, 56, 817-846.
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Acc. Chem. Res.
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Montgomery, J.1
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14
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0033855773
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Reviews: (a) Tamaru, Y. J. Organomet. Chem. 1999, 576, 215-231; (b) Montgomery, J. Acc. Chem. Res. 2000, 33, 467-473; (c) Ikeda, S.-i. Acc. Chem. Res. 2000, 33, 511-519; (d) Houpis, I. N.; Lee, J. Tetrahedron 2000, 56, 817-846.
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Acc. Chem. Res.
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Ikeda, S.-I.1
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15
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0034603026
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Reviews: (a) Tamaru, Y. J. Organomet. Chem. 1999, 576, 215-231; (b) Montgomery, J. Acc. Chem. Res. 2000, 33, 467-473; (c) Ikeda, S.-i. Acc. Chem. Res. 2000, 33, 511-519; (d) Houpis, I. N.; Lee, J. Tetrahedron 2000, 56, 817-846.
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Tetrahedron
, vol.56
, pp. 817-846
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Houpis, I.N.1
Lee, J.2
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16
-
-
85030948894
-
-
4 and a highly enantioselective variant of this transformation is under development
-
4 and a highly enantioselective variant of this transformation is under development.
-
-
-
-
17
-
-
0037182699
-
-
Catalytic, stereoselective three-component assembly of tetrahydrofurans by way of carbonyl ylide dipolar cycloaddition:
-
Catalytic, stereoselective three-component assembly of tetrahydrofurans by way of carbonyl ylide dipolar cycloaddition: Skaggs A.J., Lin E.Y., Jamison T.F. Org. Lett. 4:2002;2277-2280.
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Org. Lett.
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, pp. 2277-2280
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Skaggs, A.J.1
Lin, E.Y.2
Jamison, T.F.3
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18
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0027392308
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Terpestacin: (a) Iimura, S.; Oka, M.; Narita, Y.; Konishi, M.; Kakisawa, H.; Gao, Q.; Oki, T. Tetrahedron Lett. 1993, 34, 493-496; (b) Oka, M.; Iimura, S.; Tenmyo, O.; Sawada, Y.; Sugawara, M.; Ohkusa, N.; Yamamoto, H.; Kawano, K.; Hu, S.-L.; Fukagawa, Y.; Oki, T. J. Antibiotics 1993, 46, 367-373; (c) Oka, M.; Iimura, S.; Narita, Y.; Furumai, T.; Konishi, M.; Oki, T.; Gao, Q.; Kakisawa, H. J. Org. Chem. 1993, 58, 1875-1881.
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Tetrahedron Lett.
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Iimura, S.1
Oka, M.2
Narita, Y.3
Konishi, M.4
Kakisawa, H.5
Gao, Q.6
Oki, T.7
-
19
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0027232079
-
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Terpestacin: (a) Iimura, S.; Oka, M.; Narita, Y.; Konishi, M.; Kakisawa, H.; Gao, Q.; Oki, T. Tetrahedron Lett. 1993, 34, 493-496; (b) Oka, M.; Iimura, S.; Tenmyo, O.; Sawada, Y.; Sugawara, M.; Ohkusa, N.; Yamamoto, H.; Kawano, K.; Hu, S.-L.; Fukagawa, Y.; Oki, T. J. Antibiotics 1993, 46, 367-373; (c) Oka, M.; Iimura, S.; Narita, Y.; Furumai, T.; Konishi, M.; Oki, T.; Gao, Q.; Kakisawa, H. J. Org. Chem. 1993, 58, 1875-1881.
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J. Antibiotics
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Oka, M.1
Iimura, S.2
Tenmyo, O.3
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Sugawara, M.5
Ohkusa, N.6
Yamamoto, H.7
Kawano, K.8
Hu, S.-L.9
Fukagawa, Y.10
Oki, T.11
-
20
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0027189919
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Terpestacin: (a) Iimura, S.; Oka, M.; Narita, Y.; Konishi, M.; Kakisawa, H.; Gao, Q.; Oki, T. Tetrahedron Lett. 1993, 34, 493-496; (b) Oka, M.; Iimura, S.; Tenmyo, O.; Sawada, Y.; Sugawara, M.; Ohkusa, N.; Yamamoto, H.; Kawano, K.; Hu, S.-L.; Fukagawa, Y.; Oki, T. J. Antibiotics 1993, 46, 367-373; (c) Oka, M.; Iimura, S.; Narita, Y.; Furumai, T.; Konishi, M.; Oki, T.; Gao, Q.; Kakisawa, H. J. Org. Chem. 1993, 58, 1875-1881.
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Oka, M.1
Iimura, S.2
Narita, Y.3
Furumai, T.4
Konishi, M.5
Oki, T.6
Gao, Q.7
Kakisawa, H.8
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22
-
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0029049468
-
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Epothilones:
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Epothilones: Bollag D.M., McQueney P.A., Zhu J., Hensens O., Koupal L., Liesch J., Goetz M., Lazarides E., Woods C.M. Cancer Res. 55:1995;2325-2333.
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Liesch, J.6
Goetz, M.7
Lazarides, E.8
Woods, C.M.9
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23
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0023264587
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FK-506:
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FK-506: Tanaka H., Kuroda A., Marusawa H., Hatanaka H., Kino T., Goto T., Hashimoto M., Taga T. J. Am. Chem. Soc. 109:1987;5031-5033.
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Tanaka, H.1
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Taga, T.8
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24
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0000080952
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Trost, B. M., Ed.; Pergamon: New York, Chapter 4.6
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For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Comprehensive Organic Synthesis
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, pp. 873-908
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Brückner, R.1
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25
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0000746177
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Chapter 7.1
-
For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Comprehensive Organic Synthesis
, vol.5
, pp. 785-826
-
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Hill, R.K.1
-
26
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0000217402
-
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Chapter 7.2
-
For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Comprehensive Organic Synthesis
, vol.5
, pp. 827-873
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Wipf, P.1
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27
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0000276556
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-
For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Comprehensive Organic Synthesis
, vol.4
, pp. 585
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Godleski, S.A.1
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28
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0000458209
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For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Chem. Rev.
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Hoveyda, A.H.1
Evans, D.A.2
Fu, G.C.3
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29
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0000220284
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Wiley: New York
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For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Organic Reactions
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Lipshutz, B.H.1
Sengupta, S.2
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30
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0001626504
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For reviews of useful reactions of allylic alcohols: (a) Brückner, R. In Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon: New York, 1991; Vol. 6, Chapter 4.6, pp. 873-908; (b) Hill, R. K. ibid. Vol. 5, Chapter 7.1, pp. 785-826; (c) Wipf, P. ibid. Vol. 5, Chapter 7.2, pp. 827-873; (d) Godleski, S. A., ibid. Vol. 4, p. 585; (e) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370; (f) Lipshutz, B. H.; Sengupta, S. In Organic Reactions; Wiley: New York, 1992; Vol. 41, p. 135; (g) Overman, L. E. Acc. Chem. Res. 1992, 25, 352.
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Overman, L.E.1
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33
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0000767710
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Crowe has also reported one example of a catalytic alkyne/aldehyde reductive cyclization:
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Crowe has also reported one example of a catalytic alkyne/aldehyde reductive cyclization: Crowe W.E., Rachita M.J. J. Am. Chem. Soc. 117:1995;6787-6788.
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Crowe, W.E.1
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Kataoka Y., Miyai J., Oshima K., Takai K., Utimoto K. J. Org. Chem. 57:1992;1973-1981.
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40
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0035809288
-
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Oxanickella(II)cyclopentenes have not been characterized, but an X-ray structure of a related Ni(II)-O enolate has been reported:
-
Oxanickella(II)cyclopentenes have not been characterized, but an X-ray structure of a related Ni(II)-O enolate has been reported: Amarasinghe K.K.D., Chowdhury S.K., Heeg M.J., Montgomery J. Organometallics. 20:2001;370.
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Amarasinghe, K.K.D.1
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41
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Recent method of complementary regioselectivity for terminal alkynes:
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3: Senaratne, K. P. A. Synthesis of cycloalkyldiarylphosphines. US Patent 5,710,340, April 29, 1996.
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See also: (a) Trost, B. M.; Pinkerton, A. B. J. Am. Chem. Soc. 2002, 124, 7376-7389; (b) Dünkelmann, P.; Kolter-Jung, D.; Nitsche, A.; Demir, A. S. ; Siegert, P.; Lingen, B.; Baumann, M.; Pohl, M.; Müller, M. J. Am. Chem. Soc. 2002, 124, 12084-12085.
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See also: (a) Trost, B. M.; Pinkerton, A. B. J. Am. Chem. Soc. 2002, 124, 7376-7389; (b) Dünkelmann, P.; Kolter-Jung, D.; Nitsche, A.; Demir, A. S. ; Siegert, P.; Lingen, B.; Baumann, M.; Pohl, M.; Müller, M. J. Am. Chem. Soc. 2002, 124, 12084-12085.
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Dünkelmann, P.1
Kolter-Jung, D.2
Nitsche, A.3
Demir, A.S.4
Siegert, P.5
Lingen, B.6
Baumann, M.7
Pohl, M.8
Müller, M.9
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Ethylene and trimethylene oxides
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Elderfield, R. C., Ed.; Wiley: New York
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The selectivity trends in ring-opening reactions of aryloxiranes often differ from those involving alkyloxiranes: (a) Winstein, S.; Henderson, R. B. Ethylene and Trimethylene Oxides. In Heterocyclic Compounds, Elderfield, R. C., Ed.; Wiley: New York, 1950; Vol. 1; (b) Parker, R. E.; Isaacs, N. S. Chem. Rev. 1959, 59, 737-799; (c) Wohl, R. A. Chimia 1974, 28, 1-5.
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33947470048
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The selectivity trends in ring-opening reactions of aryloxiranes often differ from those involving alkyloxiranes: (a) Winstein, S.; Henderson, R. B. Ethylene and Trimethylene Oxides. In Heterocyclic Compounds, Elderfield, R. C., Ed.; Wiley: New York, 1950; Vol. 1; (b) Parker, R. E.; Isaacs, N. S. Chem. Rev. 1959, 59, 737-799; (c) Wohl, R. A. Chimia 1974, 28, 1-5.
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Parker, R.E.1
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The selectivity trends in ring-opening reactions of aryloxiranes often differ from those involving alkyloxiranes: (a) Winstein, S.; Henderson, R. B. Ethylene and Trimethylene Oxides. In Heterocyclic Compounds, Elderfield, R. C., Ed.; Wiley: New York, 1950; Vol. 1; (b) Parker, R. E.; Isaacs, N. S. Chem. Rev. 1959, 59, 737-799; (c) Wohl, R. A. Chimia 1974, 28, 1-5.
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Wohl, R.A.1
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Notable exceptions (catalyst-controlled endo selectivity): (a) Janda, K. D.; Shevlin, C. G.; Lerner, R. A. Science 1993, 259, 490-493; (b) Wu, M. H.; Hansen, K. B.; Jacobsen, E. N. Angew. Chem., Int. Ed. 1997, 38, 2012-2014.
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Notable exceptions (catalyst-controlled endo selectivity): (a) Janda, K. D.; Shevlin, C. G.; Lerner, R. A. Science 1993, 259, 490-493; (b) Wu, M. H.; Hansen, K. B.; Jacobsen, E. N. Angew. Chem., Int. Ed. 1997, 38, 2012-2014.
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Roush, W.R.1
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71
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0033583756
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Prepared from propargylamine hydrochloride:
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Prepared from propargylamine hydrochloride: Khan S.I., Grinstaff M.W. J. Am. Chem. Soc. 121:1999;4704-4705.
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(1999)
J. Am. Chem. Soc.
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Khan, S.I.1
Grinstaff, M.W.2
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