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

Journal of Natural Products

Volumn 70, Issue 1, 2007, Pages 75-82

  Han, Dongmei ^a   Försterling, F Holger ^a   Deschamps, Jeffrey R ^b   Parrish, Damon ^b   Liu, Xiaoxiang ^a   Yin, Wenyuan ^a   Huang, Shengming ^a   Cook, James M ^a  

^a UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

^b NAVAL RESEARCH LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BENZYL DERIVATIVE;

ARTICLE; CRYSTAL STRUCTURE; DIASTEREOISOMER; EPIMERIZATION; ISOMERIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PICTET SPENGLER REACTION; STEREOISOMERISM; X RAY CRYSTALLOGRAPHY;

BENZYL COMPOUNDS; CRYSTALLOGRAPHY, X-RAY; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 33847061595     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np060391g     Document Type: Article

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40. Please see the Supporting Information for materials and general instrumentation.