MeNBOMe [Reaxys, All Preps (14); 2016-01-02]

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15 reactions in Reaxys

2016-01-02 07h:35m:30s (EST)

ALK

1. Query

N CYC O ALK

Search as: As drawn 2. Query

(1. Query) AND itemno in (1,6,7,8,9,10,14)

15 reactions in Reaxys

2016-01-02 07h:38m:32s (EST)

3. Query

LAST_RESULT AND NOT itemno in (15)

14 reactions in Reaxys

2016-01-02 07h:52m:35s (EST)

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O H 2N

N O

O

O Cl

H

N

N

Rx-ID: 9168070 View in Reaxys 1/14 Yield

Conditions & References With hydrogenchloride, ammonium chloride, iron in acetone, T= 45 °C Liu, Hong; Ji, Ming; Luo, Xiaomin; Shen, Jianhua; Huang, Xiaoqin; Hua, Weiyi; Jiang, Hualiang; Chen, Kaixian; Journal of Medicinal Chemistry; vol. 45; nb. 14; (2002); p. 2953 - 2969 View in Reaxys

NH

H 2N

O

N

O S Cl

Cl

N

O

O

S

O

H

O

Rx-ID: 9143376 View in Reaxys 2/14 Yield

Conditions & References With triethylamine in dichloromethane Liu, Hong; Ji, Ming; Luo, Xiaomin; Shen, Jianhua; Huang, Xiaoqin; Hua, Weiyi; Jiang, Hualiang; Chen, Kaixian; Journal of Medicinal Chemistry; vol. 45; nb. 14; (2002); p. 2953 - 2969 View in Reaxys

HO O –O

N+

S

H N

O

O

O

O

O

O

OH O

N

O

N

Rx-ID: 2424796 View in Reaxys 3/14 Yield

Conditions & References

15 %, 60 % With benzene-sulfonate Golodnyuk, T. I.; Vinogradova, V. I.; Yunusov, M. S.; Chemistry of Natural Compounds; vol. 26; nb. 2; (1990); p.

232 - 233; Khimiya Prirodnykh Soedinenii; nb. 2; (1990); p. 281 - 282 View in Reaxys 60 %, 15 % With benzene-sulfonate Golodnyuk, T. I.; Vinogradova, V. I.; Yunusov, M. S.; Chemistry of Natural Compounds; vol. 26; nb. 2; (1990); p.

232 - 233; Khimiya Prirodnykh Soedinenii; nb. 2; (1990); p. 281 - 282 View in Reaxys

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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NH 2

O N O O

O

O

O O

Rx-ID: 18236440 View in Reaxys 4/14 Yield

Conditions & References Reaction Steps: 3 1: benzene / Heating 2: NaBH4 / methanol / 0 - 5 °C 3: 2.) NaBH4 / 1.) methanol, reflux, 2 h, 2.) methanol With sodium tetrahydroborate in methanol, benzene Vinogradova, V. I.; Golodnyuk, T. I.; Tulyaganov, N.; Yunusov, M. S.; Baratov, N. Yu.; Chemistry of Natural Compounds; vol. 29; nb. 3; (1993); p. 341 - 345; Khimiya Prirodnykh Soedinenii; nb. 3; (1993); p. 404 - 409 View in Reaxys

O N

O

O

O O O

Rx-ID: 18237926 View in Reaxys 5/14 Yield

Conditions & References Reaction Steps: 3 1: benzene / Heating 2: NaBH4 / methanol / 0 - 5 °C 3: 2.) NaBH4 / 1.) methanol, reflux, 2 h, 2.) methanol With sodium tetrahydroborate in methanol, benzene Vinogradova, V. I.; Golodnyuk, T. I.; Tulyaganov, N.; Yunusov, M. S.; Baratov, N. Yu.; Chemistry of Natural Compounds; vol. 29; nb. 3; (1993); p. 341 - 345; Khimiya Prirodnykh Soedinenii; nb. 3; (1993); p. 404 - 409 View in Reaxys

O

O N

N

O

O

O O

O O

Rx-ID: 18249705 View in Reaxys 6/14 Yield

Conditions & References Reaction Steps: 2 1: NaBH4 / methanol / 0 - 5 °C 2: 2.) NaBH4 / 1.) methanol, reflux, 2 h, 2.) methanol With sodium tetrahydroborate in methanol

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Vinogradova, V. I.; Golodnyuk, T. I.; Tulyaganov, N.; Yunusov, M. S.; Baratov, N. Yu.; Chemistry of Natural Compounds; vol. 29; nb. 3; (1993); p. 341 - 345; Khimiya Prirodnykh Soedinenii; nb. 3; (1993); p. 404 - 409 View in Reaxys

O

O

N

N O

O

O Cl

O

O

H

N H

N

Rx-ID: 9122923 View in Reaxys 7/14 Yield

Conditions & References With 88percent formic acid, Heating Liu, Hong; Ji, Ming; Luo, Xiaomin; Shen, Jianhua; Huang, Xiaoqin; Hua, Weiyi; Jiang, Hualiang; Chen, Kaixian; Journal of Medicinal Chemistry; vol. 45; nb. 14; (2002); p. 2953 - 2969 View in Reaxys

H 2N

O

N O

O

O

O

Rx-ID: 18188267 View in Reaxys 8/14 Yield

Conditions & References Reaction Steps: 2 1: 2.) NaBH4 / 1.) C6H6, reflux, 2.) CH3OH 2: 2.) NaBH4 / 1.) CH3OH, reflux, 1 h With sodium tetrahydroborate Vinogradova, V. I.; Golodnyuk, T. I.; Yunusov, M. S.; Suleimanova, G. A.; Tulyaganov, N.; Chemistry of Natural Compounds; vol. 29; nb. 5; (1993); p. 654 - 657; Khimiya Prirodnykh Soedinenii; nb. 5; (1993); p. 736 - 740 View in Reaxys

O O

O

O O

N

NH 2

Rx-ID: 18191369 View in Reaxys 9/14 Yield

Conditions & References Reaction Steps: 2 1: 2.) NaBH4 / 1.) C6H6, reflux, 2.) CH3OH 2: 2.) NaBH4 / 1.) CH3OH, reflux, 1 h With sodium tetrahydroborate Vinogradova, V. I.; Golodnyuk, T. I.; Yunusov, M. S.; Suleimanova, G. A.; Tulyaganov, N.; Chemistry of Natural Compounds; vol. 29; nb. 5; (1993); p. 654 - 657; Khimiya Prirodnykh Soedinenii; nb. 5; (1993); p. 736 - 740 View in Reaxys

O O O

O

N

O

Rx-ID: 18196103 View in Reaxys 10/14 Yield

Conditions & References Reaction Steps: 2

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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1: 2.) NaBH4 / 1.) C6H6, reflux, 2.) CH3OH 2: 2.) NaBH4 / 1.) CH3OH, reflux, 1 h With sodium tetrahydroborate Vinogradova, V. I.; Golodnyuk, T. I.; Yunusov, M. S.; Suleimanova, G. A.; Tulyaganov, N.; Chemistry of Natural Compounds; vol. 29; nb. 5; (1993); p. 654 - 657; Khimiya Prirodnykh Soedinenii; nb. 5; (1993); p. 736 - 740 View in Reaxys

N

O

O

O

O

O

Rx-ID: 18196105 View in Reaxys 11/14 Yield

Conditions & References Reaction Steps: 2 1: 2.) NaBH4 / 1.) C6H6, reflux, 2.) CH3OH 2: 2.) NaBH4 / 1.) CH3OH, reflux, 1 h With sodium tetrahydroborate Vinogradova, V. I.; Golodnyuk, T. I.; Yunusov, M. S.; Suleimanova, G. A.; Tulyaganov, N.; Chemistry of Natural Compounds; vol. 29; nb. 5; (1993); p. 654 - 657; Khimiya Prirodnykh Soedinenii; nb. 5; (1993); p. 736 - 740 View in Reaxys

O

O O

O

O

O

N H

O

N

Rx-ID: 3948256 View in Reaxys 12/14 Yield

Conditions & References With sodium tetrahydroborate, 1.) CH3OH, reflux, 1 h, Multistep reaction Vinogradova, V. I.; Golodnyuk, T. I.; Yunusov, M. S.; Suleimanova, G. A.; Tulyaganov, N.; Chemistry of Natural Compounds; vol. 29; nb. 5; (1993); p. 654 - 657; Khimiya Prirodnykh Soedinenii; nb. 5; (1993); p. 736 - 740 View in Reaxys

H N

O O

N

O O

O

O O

Rx-ID: 3948381 View in Reaxys 13/14 Yield

Conditions & References With sodium tetrahydroborate, 1.) CH3OH, reflux, 1 h, Multistep reaction Vinogradova, V. I.; Golodnyuk, T. I.; Yunusov, M. S.; Suleimanova, G. A.; Tulyaganov, N.; Chemistry of Natural Compounds; vol. 29; nb. 5; (1993); p. 654 - 657; Khimiya Prirodnykh Soedinenii; nb. 5; (1993); p. 736 - 740 View in Reaxys

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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O

O NH

N

O

O

O

O O

O O

Rx-ID: 3948385 View in Reaxys 14/14 Yield

Conditions & References With sodium tetrahydroborate, 1.) methanol, reflux, 2 h, 2.) methanol, Yield given. Multistep reaction Vinogradova, V. I.; Golodnyuk, T. I.; Tulyaganov, N.; Yunusov, M. S.; Baratov, N. Yu.; Chemistry of Natural Compounds; vol. 29; nb. 3; (1993); p. 341 - 345; Khimiya Prirodnykh Soedinenii; nb. 3; (1993); p. 404 - 409 View in Reaxys

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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