Total synthesis and biological properties of novel antineoplastic (chloromethyl)furanoindolines: an asymmetric hydroboration mediated synthesis of the alkylation subunits-Reference-Cited by-同舟云学术

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Total synthesis and biological properties of novel antineoplastic (chloromethyl)furanoindolines: an asymmetric hydroboration mediated synthesis of the alkylation subunits

Published:1994-01 Issue:2 Volume:37 Page:232-239
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Mohamadi Fariborz,Spees Michael M.,Staten Gilbert S.,Marder Philip,Kipka Julia K.,Johnson David A.,Boger Dale L.,Zarrinmayeh Hamideh

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm00028a005

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1. Amino DSA analogues as payloads for antibody-drug conjugates with multiple sites for conjugation. Initial studies and solid phase synthesis;Tetrahedron Letters;2021-05

2. Stereoselective Synthesis of Dihydrofuranoindoles via the Friedel–Crafts Alkylation/Annulation Cascade Process;The Journal of Organic Chemistry;2020-08-24

3. C-H activation: a Critical Evaluation of a Published Method and its Application Towards Inherently Chiral Calix[4]arenes;S AFR J CHEM-S-AFR T;2020

4. The Difference a Single Atom Can Make: Synthesis and Design at the Chemistry–Biology Interface;The Journal of Organic Chemistry;2017-10-13

5. Synthesis and evaluation of duocarmycin SA analogs incorporating the methyl 1,2,8,8a-tetrahydrocyclopropa[c]imidazolo[4,5-e]indol-4-one-6-carboxylate (CImI) alkylation subunit;Bioorganic & Medicinal Chemistry;2016-10

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