Chiral synthesis of trans-1-aminoindolo [2, 3-a] quinolizidine and trans-1-aminobenzo [a] quinolizidine derivatives from L-pyroglutamic acid
YS Lee, DJ Cho, SN Kim, JH Choi…
Index: Lee, Yong Sup; Cho, Dae Joo; Kim, Sun Nam; Choi, Jung Hoon; Park, Hokoon Journal of Organic Chemistry, 1999 , vol. 64, # 26 p. 9727 - 9730
Full Text: HTML
Citation Number: 21
Abstract
Benzo [a] quinolizidine and indolo [2, 3-a] quinolizidine ring systems are key subunits of naturally occurring isoquinoline and indole alkaloids. 1 1-Aminoindolo [2, 3-a]-quinolizidines have been used as intermediates in the synthesis of the pharmacologically interesting pentacyclic compound 62 and (E)-azaeburnane derivatives. 3 Benzo-[a] quinolizidines, including 1-aminobenzo [a] quinolizidines, have also served as intermediates in the ...
Related Articles:
[Anelli, Pier Lucio; Brocchetta, Marino; Lattuada, Luciano; Manfredi, Giuseppe; Morosini, Pierfrancesco; Murru, Marcella; Palano, Daniela; Sipioni, Marco; Visigalli, Massimo Organic Process Research and Development, 2009 , vol. 13, # 4 p. 739 - 746]
Convenient N-Protection of L-Pyroglutamic Acid Esters
[Jain, Rahul Organic Preparations and Procedures International, 2001 , vol. 33, # 4 p. 405 - 409]
[Adams, David R.; Bailey, Patrick D.; Collier, Ian D.; Heffernan, John D.; Stokes, Stephen Chemical Communications, 1996 , # 3 p. 349 - 350]