Diastereoselective Spirocyclization of Imines of 2‐Substituted 1H‐Indole‐3‐ethylamines ( = Trypatamines): Variation of the electrophile and the substituent at C(2) and its influence on the steric outcome. 6th Communication on indoles, indolenines, and indolines

Helvetica Chimica Acta

Volumn 75, Issue 1, 1992, Pages 282-287

  Freund, Ralf ^b,c   Martinović, Suzanna ^a   Bernauer, Karl ^a,b  

^a F HOFFMANN LA ROCHE LTD   (Switzerland)

^b UNIVERSITY OF ZURICH   (Switzerland)

^c UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TRYPTAMINE DERIVATIVE;

ARTICLE; REACTION ANALYSIS; SYNTHESIS;

EID: 0026571677     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.19920750124     Document Type: Article

References (6)

1. Diastereoselective Spirocyclization ofC-(Alkyloxycarbonyl)formimines of 2-Substituted 1HIndole-3-ethanamines (= Tryptamines): Basic Studies. 5th Communication on Indoles, Indolenines, and Indolines
2. Further studies on the use of multi-substituted benzenesulfonyl groups for protection of the guanidino function of arginine.
3. Neue Synthesen von 2-Acylbenzofuranen, 2-Acylindolen, 2-Indolycarbonsäureestern und 2-Chinolonen durch intramolekulare Wittig-Reaktion
4. Synthesis of Esters of 3-(2-Aminoethyl)-1H-indole-2-acetic Acid and 3-(2-aminoethyl)-1H-indole-2-malonic acid (= 2-[3-(2-aminoethyl)-1H-indol-2-yl]propanedioic acid) 4th communication on indoles, indolenines, and indolines