27613-27-0Relevant articles and documents
Synthesis, Rearrangement, and Hauser Annulation of 3-Isocyanophthalides
Mal, Dipakranjan,Ghosh, Ketaki,Chakraborty, Soumen
, p. 2473 - 2484 (2015)
3-Isocyanoisobenzofuran-1(3H)-ones (phthalides) were prepared in two steps from the corresponding phthalaldehydic acids. The 3-isocyanoisobenzofuran-1(3H)-ones are readily rearranged to the corresponding 3-cyanoisobenzofuran-1(3H)-ones using triflic anhyd
ENEDIYNE COMPOUNDS, CONJUGATES THEREOF, AND USES AND METHODS THEREFOR
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Page/Page column, (2013/08/28)
Enediyne compounds having a structure according to formula (I), where R0, R2, R3, R4, R5, R6, and R7 are defined herein, can be used in chemotherapeutic drugs, especially in conjugates, for the treatment of diseases such as cancer.
Total synthesis of the spermidine alkaloid 13-hydroxyisocyclocelabenzine
Li, Yi,Linden, Anthony,Hesse, Manfred
, p. 579 - 591 (2007/10/03)
A convergent total synthesis of 13-hydroxyisocyclocelabenzine was developed. (3S)-Methyl 3-amino-3-phenylpropanoate (4) was used as the chiral building block. The 3,4-dihydro-4-hydroxyisoquinolin-1(2H)-one derivative (5), the key fragment for the total sy