17138-39-5Relevant academic research and scientific papers
N-fused indolines through non-carbonyl-stabilized rhodium carbenoid C-H insertion of N-aziridinyl imines
Mahoney, Stuart J.,Fillion, Eric
, p. 68 - 71 (2012/02/04)
Under rhodium catalysis, N-aziridinyl imines provided access to N-fused indolines through non-carbonyl-stabilized rhodium carbenoid C-H insertion. The utility of this methodology for the synthesis of architecturally complex heterocycles was further demonstrated by an expedient total synthesis of ( ±)-cryptaustoline (see scheme). Copyright
Use of (NHC)Pd(η3-allyl)Cl (NHC = N-Heterocyclic Carbene) in a Palladium-mediated Approach to Cryptocarya Alkaloids
C?mmerer, Simon S.,Viciu, Mihai S.,Stevens, Edwin D.,Nolan, Steven P.
, p. 1871 - 1873 (2007/10/03)
The palladium-mediated intramolecular aryl amination of 7-benzyloxy-1-(2-bromo-4,5-dimethoxy-benzyl)-1,2,3, 4-tetrahydro-6-methoxy-isoquinoline catalyzed by a recently discovered, air and moisture stable (NHC)Pd(η3-allyl)Cl (NHC = N-heterocycli
A facile route to indolo[2,1-a]isoquinolines and dibenzopyrrocoline alkaloids
Orito, Kazuhiko,Harada, Rika,Uchiito, Shiho,Tokuda, Masao
, p. 1799 - 1801 (2007/10/03)
(Formula presented) Treatment of 1-(2′-bromobenzyl)-3,4-dihydroisoquinolines 2 in the presence of K2CO3 in boiling DMF efficiently provided a variety of alkoxysubstituted indolo[2,1-a]isoquinolines 3. Application of this cyclization
A NOVEL TOTAL SYNTHESIS OF (+/-)-CRYPTAUSTOLINE, A DIBENZOPYRROCOLINE ALKALOID
Yasuda, Shingo,Hirasawa, Taeko,Yoshida, Shuji,Hanaoka, Miyoji
, p. 1682 - 1683 (2007/10/02)
(+/-)-Cryptaustoline (1), a dibenzopyrrocoline alkaloid, was efficiently synthesized from the readily available N-phenethylaniline (7) via the N-phenethyloxindole (12) or the N-phenethylindole (14) by the Bischler-Napieralski reaction or by radical cycliz
SILICON-MEDIATED ISOQUINOLINE ALKALOID SYNTHESIS: A NEW ROUTE TO THE DIBENZOPYRROCOLINE ALKALOID (+/-)-CRYPTAUSTOLINE
Takano, Seiichi,Satoh, Shigeki,Ogasawara, Kunio
, p. 1483 - 1485 (2007/10/02)
A fundamentally new synthesis of the benzopyrrocoline alkaloid (+/-)-cryptaustoline iodide (12) has been devised by employing the silicon mediated ring closure through a formal 5-Endo-Trigonal process.
