Conformational Analysis of the cis- and trans-Adducts of the Pictet−Spengler Reaction. Evidence for the Structural Basis for the C(1)−N(2) Scission Process in the cis- to trans-Isomerization-Reference-Cited by-同舟云学术

Conformational Analysis of the cis- and trans-Adducts of the Pictet−Spengler Reaction. Evidence for the Structural Basis for the C(1)−N(2) Scission Process in the cis- to trans-Isomerization

Published:2006-12-20 Issue:1 Volume:70 Page:75-82
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Han Dongmei¹,Försterling F. Holger¹,Deschamps Jeffrey R.¹,Parrish Damon¹,Liu Xiaoxiang¹,Yin Wenyuan¹,Huang Shengming¹,Cook James M.¹

Affiliation:

1. Department of Chemistry, University of Wisconsin−Milwaukee, Milwaukee, Wisconsin 53211, and Laboratory for the Structure of Matter, Naval Research Laboratory, Washington, D.C. 20375

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/np060391g

Reference36 articles.

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4. Examples utilizing the Pictet−Spengler reaction. (a) Czerwinski, K. M.; Cook, J. M. InAdvances in Heterocyclic Natural Products Synthesis; Pearson, W., Ed.; JAI Press: Greenwich, CT, 1996; Vol. 3, pp 217−277. (b) Ashley, E. R.; Cruz, E. G.; Stoltz, B. M.J. Am. Chem. Soc.2003,125, 15000−15001. (c) Niesen, T. E.; Meldal, M.J. Org. Chem.2004,69, 3765−3773. (d) Bunin, B. A.; Dener, J. M.; Kelly, D. E.; Paras, N. A.; Tario, J. D.; Tushup, S. P.J. Comb. Chem.2004,6, 487−496.

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