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0001446504
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Leading references: (a) Heusler K., Kalvoda J. Angew. Chem., Int. Ed. Engl. 3:1964;525-538 (b) Mihailović M.L., Čeković Ž. Synthesis. 1970;209-224 (c) Kalvoda J., Heusler K. Synthesis. 1971;501-526 (d) Barton D.H.R. Pure Appl. Chem. 16:1968;1 (e) Hesse R.H. Adv. Free Radical Chem. 3:1969;83 (f) Majetich G., Wheless K. Tetrahedron (Rep. No. 375). 51:1995;7095-7129 (g) Robertson J., Pillai J., Lush R.K. Chem. Soc. Rev. 30:2001;94-103 (h) Wolff M.E. Chem. Rev. 63:1963;55-64.
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Kalvoda, J.1
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4
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0003014165
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Leading references: (a) Heusler K., Kalvoda J. Angew. Chem., Int. Ed. Engl. 3:1964;525-538 (b) Mihailović M.L., Čeković Ž. Synthesis. 1970;209-224 (c) Kalvoda J., Heusler K. Synthesis. 1971;501-526 (d) Barton D.H.R. Pure Appl. Chem. 16:1968;1 (e) Hesse R.H. Adv. Free Radical Chem. 3:1969;83 (f) Majetich G., Wheless K. Tetrahedron (Rep. No. 375). 51:1995;7095-7129 (g) Robertson J., Pillai J., Lush R.K. Chem. Soc. Rev. 30:2001;94-103 (h) Wolff M.E. Chem. Rev. 63:1963;55-64.
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Leading references: (a) Heusler K., Kalvoda J. Angew. Chem., Int. Ed. Engl. 3:1964;525-538 (b) Mihailović M.L., Čeković Ž. Synthesis. 1970;209-224 (c) Kalvoda J., Heusler K. Synthesis. 1971;501-526 (d) Barton D.H.R. Pure Appl. Chem. 16:1968;1 (e) Hesse R.H. Adv. Free Radical Chem. 3:1969;83 (f) Majetich G., Wheless K. Tetrahedron (Rep. No. 375). 51:1995;7095-7129 (g) Robertson J., Pillai J., Lush R.K. Chem. Soc. Rev. 30:2001;94-103 (h) Wolff M.E. Chem. Rev. 63:1963;55-64.
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1 H NMR spectrum of the mixture of isomers 15 two signals were obtained for hydrogens next to the phenylthio group, signals at δ=2.84 ppm belong to the trans-isomer 15a and at δ=3.50 ppm are from the cis-isomer 15b and they possess different coupling constants. This is in agreement with described results. Eliel, E.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley: New York, 1994, pp 712.
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1 H NMR spectrum of the mixture of isomers 15 two signals were obtained for hydrogens next to the phenylthio group, signals at δ=2.84 ppm belong to the trans-isomer 15a and at δ=3.50 ppm are from the cis-isomer 15b and they possess different coupling constants. This is in agreement with described results. Eliel, E.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley: New York, 1994, pp 712.
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