Todd:Catalytic, Asymmetric Pictet-Spengler Reaction: Difference between revisions

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List reported the first Bronsted acid-catalyzed enantioselective Pictet-Spengler reaction in 2006.(10.1021/ja057444l) Chiral, substituted phosphoric acids were shown to be effective in the PS cyclization of tryptamines with a number of aliphatic and aromatic aldehydes. The diester functionality was found to be necessary, presumably due to promotion of a clean reaction through the Thorpe-Ingold effect, and prevent side reactions such as an aldol reaction what was observed when this group was absent. Typically lower yields were observed when the methoxy group was absent from the tryptamine.<br>
List reported the first Bronsted acid-catalyzed enantioselective Pictet-Spengler reaction in 2006.(10.1021/ja057444l) Chiral, substituted phosphoric acids were shown to be effective in the PS cyclization of tryptamines with a number of aliphatic and aromatic aldehydes. The diester functionality was found to be necessary, presumably due to promotion of a clean reaction through the Thorpe-Ingold effect, and prevent side reactions such as an aldol reaction what was observed when this group was absent. Typically lower yields were observed when the methoxy group was absent from the tryptamine.<br>


[[Image:2006 List JACS.png|thumb|center|750px|'''Scheme (List 2006)'''. Chiral Phosphoric Acid PS Cyclization of Typtamine Diesters]]


To Do:<br>
Early work on addition reactions to aldimines catalyzed by binaphthol-derived chiral phosphoric acids: Akiyama et al ((a) Angew. Chem., Int. Ed. 2004, 43, 1566-1568; (b) Org. Lett. 2005, 7, 2583-2585; (c) Akiyama, T. PCT Int. Appl. WO 200409675, 2004; (d) Adv. Synth. Catal. 2005, 347, 1523-1526. And Terada et al ((a) J. Am. Chem. Soc. 2004, 126, 5356-5357. (b) J. Am. Chem. Soc. 2004, 126, 11804-11805. (c) J. Am. Chem. Soc. 2005, 127, 9360-9361; (d) Terada, M.; Uraguchi, D.; Sorimachi, K.; Shimizu, H. PCT Int. Appl. WO 2005070875, 2005.).<br>
Early work on addition reactions to aldimines catalyzed by binaphthol-derived chiral phosphoric acids: Akiyama et al ((a) Angew. Chem., Int. Ed. 2004, 43, 1566-1568; (b) Org. Lett. 2005, 7, 2583-2585; (c) Akiyama, T. PCT Int. Appl. WO 200409675, 2004; (d) Adv. Synth. Catal. 2005, 347, 1523-1526. And Terada et al ((a) J. Am. Chem. Soc. 2004, 126, 5356-5357. (b) J. Am. Chem. Soc. 2004, 126, 11804-11805. (c) J. Am. Chem. Soc. 2005, 127, 9360-9361; (d) Terada, M.; Uraguchi, D.; Sorimachi, K.; Shimizu, H. PCT Int. Appl. WO 2005070875, 2005.).<br>


Revision as of 04:58, 11 December 2011

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The Catalytic, Asymmetric Pictet-Spengler Reaction

Matthew H. Todd, School of Chemistry, The University of Sydney, NSW 2006, Australia

(additional authors - add alphabetically if you contribute a scheme+description. Final arbitration on authorship lies with Mat Todd

(This article is a review that acts as background to the open science project to find a catalytic, asymmetric route to praziquantel. The review is open source, meaning anyone can add and edit. When it is deemed to be up to date, error-free and well-written, it will be submitted for publication, but editing can continue here. This page is currently active - when this changes <= these words will be changed (and you can see when the last edit of this page was at the bottom). References for this page may be found in full at the Mendeley page). If you want to get in touch to ask questions please do not use email. You can use the talk page (tab above), or directly insert a question on this page with your initials, or discuss via Google+ pages: Mat, (please add other public places where you can be contacted if you contribute as an author).

Racemic/Achiral

To Do:

  • Pictet, A.; Spengler, T. Ber. Dtsch. Chem. Ges. 1911, 44, 2030-2036.
  • Tatsui, G. J. Pharm. Soc. Jpn. 1928, 48, 92.
  • Cox, E. D.; Cook, J. M. Chem. Rev. 1995, 95, 1797- 1842
  • Chrzanowska, M.; Rozwadowska, M. D. Chem. Rev. 2004, 104, 3341-3370.
  • Nature: Naoi, M.; Maruyama, W.; Nagy, G. M. Neurotoxicology 2004, 25, 193- 204

Diastereoselective

To Do:

  • Cox, E. D.; Hamaker, L. K.; Li, J.; Yu, P.; Czerwinski, K. M.; Deng, L.; Bennett, D. W.; Cook, J. M. J. Org. Chem. 1997, 62, 44-61 and references therein.
  • Czarnocki, Z.; MacLean, D. B.; Szarek, W. A. Can. J. Chem. 1986, 64, 2205-2210.
  • Czarnocki, Z.; Suh, D.; MacLean, D. B.; Hultin, P. G.; Szarek, W. A. Can. J. Chem. 1992, 70, 1555-1561.
  • Czarnocki, Z.; Mieckzkowsi, J. B.; Kiegiel, J.; Arazn ́y, Z. Tetrahyedron: Asymmetry 1995, 6, 2899-2902.
  • Waldmann, H.; Schmidt, G.; Henke, H.; Burkard, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 2402-2403.
  • Schmidt, G.; Waldmann, H.; Henke, H.; Burkard, M. Chem. Eur. J. 1996, 2, 1566-1571.
  • Gremmen, C.; Willemse, B.; Wanner, M. J.; Koomen, G.-J. Org. Lett. 2000, 2, 1955-1958.
  • Gremmen, C.; Wanner, M. J.; Koomen, G.-J. Tetrahedron Lett. 2001, 42, 8885-8888.
  • Tsuji, R.; Nakagawa, M.; Nishida, A. Tetrahedron: Asymmetry 2003, 14, 177- 180.

Enantioselective

Lewis Acids

To Do:

  • Yamada, H.; Kawate, T.; Matsumizu, M.; Nishida, A.; Yamaguchi, K.; Nakagawa, M. J. Org. Chem. 1998, 63, 6348-6354
  • Hino, T.; Nakagawa, M. Heterocycles 1998, 49, 499-531.

Bronsted Acids

List reported the first Bronsted acid-catalyzed enantioselective Pictet-Spengler reaction in 2006.(10.1021/ja057444l) Chiral, substituted phosphoric acids were shown to be effective in the PS cyclization of tryptamines with a number of aliphatic and aromatic aldehydes. The diester functionality was found to be necessary, presumably due to promotion of a clean reaction through the Thorpe-Ingold effect, and prevent side reactions such as an aldol reaction what was observed when this group was absent. Typically lower yields were observed when the methoxy group was absent from the tryptamine.

Scheme (List 2006). Chiral Phosphoric Acid PS Cyclization of Typtamine Diesters

To Do:
Early work on addition reactions to aldimines catalyzed by binaphthol-derived chiral phosphoric acids: Akiyama et al ((a) Angew. Chem., Int. Ed. 2004, 43, 1566-1568; (b) Org. Lett. 2005, 7, 2583-2585; (c) Akiyama, T. PCT Int. Appl. WO 200409675, 2004; (d) Adv. Synth. Catal. 2005, 347, 1523-1526. And Terada et al ((a) J. Am. Chem. Soc. 2004, 126, 5356-5357. (b) J. Am. Chem. Soc. 2004, 126, 11804-11805. (c) J. Am. Chem. Soc. 2005, 127, 9360-9361; (d) Terada, M.; Uraguchi, D.; Sorimachi, K.; Shimizu, H. PCT Int. Appl. WO 2005070875, 2005.).

The strengths of these chiral phosphoric acids is governed by...?

Organocatalysts

To Do:

  • Taylor, M. S.; Jacobsen, E. N. J. Am. Chem. Soc. 2004, 126, 10558- 10559.

Miscellaneous Other Systems/Ones not yet used for PS

Conclusions, and what's needed in this field

References

Papers included in the review should be listed here when the description of the science is complete. The papers may be found in full at the Mendeley page)

  • Catalytic Asymmetric Pictet-Spengler Reaction, J. Seayad, A. M. Seayad and B. List, J. Am. Chem. Soc. 2006, 128, 1086-1087. Paper
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