TY - JOUR
T1 - Synthesis of nuevamine aza-analogues by a sequence
T2 - I-MCR-aza-Diels-Alder- Pictet-Spengler
AU - Islas-Jácome, Alejandro
AU - Cárdenas-Galindo, Luis E.
AU - Jerezano, Alberto V.
AU - Tamariz, Joaquín
AU - González-Zamora, Eduardo
AU - Gámez-Montaño, Rocío
PY - 2012
Y1 - 2012
N2 - A series of nuevamine aza-analogues were prepared in moderate to good yields in two reaction steps. The synthetic strategy involves an isonitrile-based multicomponent reaction, including an aza-Diels-Alder cycloaddition and Pictet-Spengler reaction as postcondensation.
AB - A series of nuevamine aza-analogues were prepared in moderate to good yields in two reaction steps. The synthetic strategy involves an isonitrile-based multicomponent reaction, including an aza-Diels-Alder cycloaddition and Pictet-Spengler reaction as postcondensation.
KW - I-MCR
KW - Pictet-Spengler cyclization
KW - S-oxidation
KW - aza-Diels-Alder
KW - nuevamine aza-analogue
UR - http://www.scopus.com/inward/record.url?scp=84869389028&partnerID=8YFLogxK
U2 - 10.1055/s-0032-1317622
DO - 10.1055/s-0032-1317622
M3 - Artículo
SN - 0936-5214
VL - 23
SP - 2951
EP - 2956
JO - Synlett
JF - Synlett
IS - 20
ER -