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0010721341
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note
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2, hexane) containing the sulfur compounds (thiols, thioketones, ...). Higher yields were obtained with longer reaction times and with aldehydes. Similar experiments were performed in water : typically 10-25μmol of ketone and 1ml of a 0.1 SM sulfuric acid solution were placed in a glass ampula and purged with argon. The suspension was frozen at -78°C and 45mg (0.18mmol) of solid sodium sulfide were added. After sealing under vacuum at -20°C the ampula was heated at 100°C for a period of time extending from one week to several months after which the aqueous phase was extracted with hexane and chromatographed on silica gel prior to GC-MS analysis.
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13
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0342628442
-
-
+] (74%), 387 (7), 369 (11), 316 (100), 301 (27), 247 (20), 203 (75), 161 (42)
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+] (74%), 387 (7), 369 (11), 316 (100), 301 (27), 247 (20), 203 (75), 161 (42).
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Scheibye, S.1
Shabana, R.2
Lawesson, S.O.3
Rømming, C.4
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20
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0010677219
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-
note
-
+] (52%), 411 (6), 386 (100), 316 (54), 55 (74).
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-
-
-
21
-
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0010713476
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note
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2, hexane).
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-
-
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22
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0010721342
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in press
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12. Formation of 8 and 9 as predominant sulfides may be the result of polysulfide-catalyzed ejto-cyclisations of thiols on double bond similar to those described in Poinsot, J.; Schneckenburger, P.; Adam, P.; Schaeffer, P.; Trendel, J.; Albrecht, P. J. Chem. Soc., Chem. Commun., in press.
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Poinsot, J.1
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23
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46549103295
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Belotti, D.1
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24
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0010667536
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note
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+] (100%), 409 (50), 315 (11), 269 (14), 161 (27), 95 (20).
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-
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25
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0000242881
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15. a) Swartz, I.E.; Karic-Miller, E.; Harold, S.J. J. Am. Chem. Soc. 1982, 111, 1211-1216. Cossy, J.; Belotti, D.; Kim Cuong, N.; Chassagnard, C. Tetrahedron 1993, 49, 7691-7700.
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0027261065
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27
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0002025512
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