The use of the β-amino-alcohol-n-oxide derivatives in the synthesis of 2,3 or 4-alkyl substituted nh pyrrolidines
作者:Georges Roussi、Jidong Zhang
DOI:10.1016/s0040-4020(01)87128-3
日期:1991.1
Nonstabilizedazomethineylidesgeneratedfrom the various β-amino alcohols N-oxides 13, 17, 23 and 24 undergo [3+2] cycloaddition reactions with unactivated alkenes to afford the corresponding pyrrolidines 14a-g, 18a-g, 25 and 27 in moderate to good yields. These compounds are precursors of NH pyrrolidines substituted in position 2, 3 or 4.
[EN] FUSED TRICYCLIC COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, AND USE THEREOF<br/>[FR] COMPOSÉ TRICYCLIQUE CONDENSÉ, COMPOSITION PHARMACEUTIQUE ASSOCIÉE ET SON UTILISATION<br/>[ZH] 稠合三环类化合物、其药物组合物及用途
Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.
[EN] COMBINATIONS<br/>[FR] ASSOCIATIONS
申请人:RECURIUM IP HOLDINGS LLC
公开号:WO2021127047A1
公开(公告)日:2021-06-24
Disclosed herein are combinations of compounds for treating a disease or condition, such as cancer. A combination of compounds for treating a disease or condition can include a SERD inhibitor and a WEE1 inhibitor, along with pharmaceutically acceptable salts of any of the foregoing.