Open AccessTotal Synthesis of (+)-Rubellin C
Author(s) -
Jackson A. Gartman,
Uttam K. Tambar
Publication year - 2020
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.0c02127
Subject(s) - stereocenter , chemistry , stereochemistry , sequence (biology) , stereoselectivity , nucleus , ring (chemistry) , total synthesis , combinatorial chemistry , topology (electrical circuits) , catalysis , enantioselective synthesis , biochemistry , organic chemistry , mathematics , combinatorics , biology , microbiology and biotechnology
The rubellins are a family of stereochemically complex anthraquinoid heterodimers containing an unprecedented chemical scaffold. Although the rubellins have been known for over three decades, no total synthesis has been achieved since their discovery. Their topology is characterized by a 6-5-6 fused ring system, five neighboring stereocenters including a quaternary center all in a convoluted core, and an anthraquinone nucleus. The rubellin architecture has been shown to inhibit and reverse the aggregation of tau protein, a therapeutically relevant target for Alzheimer's disease. Herein, we describe the first stereoselective synthesis of a member of the family, (+)-rubellin C, in 16 steps. Strategic disconnections allow expedient construction of stereochemical and topological intricacy in a short sequence of borylative and transition metal-catalyzed steps.