(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇合成路线 （共 13 条）
1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
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反应条件
acetic acid; platinum Hydrogenation;
参考文献
Sondheimer et al.
Journal of the American Chemical Society, 1955 , vol. 77, p. 4145,4148
1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
→
反应条件
acetic acid; platinum Hydrogenation;
参考文献
Sondheimer et al.
Journal of the American Chemical Society, 1955 , vol. 77, p. 4145,4148
1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
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反应条件
cyclohexanone; aluminum isopropoxide; toluene
参考文献
Gist-Brocades N.V.
Patent: US4075233 A1, 1978 ;
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
Multi-step reaction with 3 steps 1: aq. N2H4, Et3N / ethanol / Heating2: I2, Et3N / tetrahydrofuran; ethanol3: Na / ethanol
参考文献
Barton,D.H.R. et al. Journal of the Chemical Society, 1962 , p. 470 - 476
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
Multi-step reaction with 2 steps 1: I2, Et3N / tetrahydrofuran; ethanol2: Na / ethanol
参考文献
Barton,D.H.R. et al. Journal of the Chemical Society, 1962 , p. 470 - 476
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
<b>Multi-step reaction with 3 steps<br /> </b>1: aq. N<sub>2</sub>H<sub>4</sub>, Et<sub>3</sub>N / ethanol / Heating<br />2: I<sub>2</sub>, Et<sub>3</sub>N / tetrahydrofuran; ethanol<br />3: Na / ethanol<br /> <br />
参考文献
Barton,D.H.R. et al. Journal of the Chemical Society, 1962 , p. 470 - 476
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
<b>Multi-step reaction with 2 steps<br /> </b>1: I<sub>2</sub>, Et<sub>3</sub>N / tetrahydrofuran; ethanol<br />2: Na / ethanol<br /> <br />
参考文献
Barton,D.H.R. et al. Journal of the Chemical Society, 1962 , p. 470 - 476
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
Stage #1: <b>With</b> <a href="#" onclick="return RXDsubstances(event, this, '610130', constants.ctx, '0')">toluene-4-sulfonic acid hydrazide</a> <b>in</b> <a href="#" onclick="return RXDsubstances(event, this, '1718733', constants.ctx, '0')">ethanol</a> <br />Bamford-Stevens Decomposition; 2 h; Reflux; <br />Stage #2: <b>With</b> <a href="#" onclick="return RXDsubstances(event, this, '3587162', constants.ctx, '0')">methyllithium</a> <b>in</b> <a href="#" onclick="return RXDsubstances(event, this, '1696894', constants.ctx, '0')">diethyl ether</a> <br />T=22°C; Bamford-Stevens Decomposition; 16.5 h; <br />
参考文献
Starkenmann, Christian; Mayenzet, Fabienne; Brauchli, Robert; Troccaz, Myriam Chemistry and Biodiversity, 2013 , vol. 10, # 12 p. 2197 - 2208
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
<b>With</b> <a href="#" onclick="return RXDsubstances(event, this, '3647881', constants.ctx, '0')">sodium</a> <b>in</b> <a href="#" onclick="return RXDsubstances(event, this, '1718733', constants.ctx, '0')">ethanol</a> <br /> <br />
参考文献
Barton,D.H.R. et al. Journal of the Chemical Society, 1962 , p. 470 - 476
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1224-94-8(3S,8S,9S,10R,13R,14S)-10,13-二甲基-2,3,4,7,8,9,11,12,14,15-十氢-1H-环戊并[a]菲-3-醇
反应条件
<b>With</b> <a href="#" onclick="return RXDsubstances(event, this, '11342940', constants.ctx, '0')">sodium hydroxide</a> <b>in</b> <a href="#" onclick="return RXDsubstances(event, this, '1098229', constants.ctx, '0')">methanol</a> <br /> <br />
参考文献
Misiti,D. et al. Gazzetta Chimica Italiana, 1968 , vol. 98, p. 1284 - 1289
