Mn-, Fe-, and Co-catalyzed radical hydrofunctionalizations of olefins

SWM Crossley, C Obradors, RM Martinez… - Chemical …, 2016 - ACS Publications
Cofactor-mimetic aerobic oxidation has conceptually merged with catalysis of syngas
reactions to form a wide range of Markovnikov-selective olefin radical …

Muscarine, imidazole, oxazole and thiazole alkaloids

Z Jin - Natural product reports, 2016 - pubs.rsc.org
Covering: July 2012 to June 2015. Previous review: Nat. Prod. Rep., 2013, 30, 869–915 The
structurally diverse imidazole-, oxazole-, and thiazole-containing secondary metabolites are …

Total synthesis of (−)-Rhodomollanol A

J Gao, P Rao, K Xu, S Wang, Y Wu… - Journal of the American …, 2020 - ACS Publications
An asymmetric approach for the first total synthesis of (−)-rhodomollanol A, a highly oxidized
diterpenoid, is described. The efficient synthetic strategy features three key …

Inner- and Outer-Sphere Cross-Coupling of High Fsp3 Fragments

S Kotesova, RA Shenvi - Accounts of Chemical Research, 2023 - ACS Publications
Conspectus Natural product research originates from a desire to explore, understand, and
perturb biological function with atomic precision. To reach these goals at all, let alone …

A global and local desymmetrization approach to the synthesis of steroidal alkaloids: stereocontrolled total synthesis of paspaline

RJ Sharpe, JS Johnson - Journal of the American Chemical …, 2015 - ACS Publications
A stereocontrolled total synthesis of the indole diterpenoid natural product paspaline is
described. Key steps include a highly diastereoselective enzymatic desymmetrization …

Total synthesis of paspaline A and emindole PB enabled by computational augmentation of a transform-guided retrosynthetic strategy

DE Kim, JE Zweig, TR Newhouse - Journal of the American …, 2019 - ACS Publications
We report the total syntheses of two indole diterpenoid natural products, paspaline A and
emindole PB. Paspaline A is synthesized in a 9-step sequence from commercially available …

Asymmetric total synthesis of the indole diterpene alkaloid paspaline

RJ Sharpe, JS Johnson - The Journal of organic chemistry, 2015 - ACS Publications
An enantioselective synthesis of the indole diterpenoid natural product paspaline is
disclosed. Critical to this approach was the implementation of stereoselective …

Enantioselective Total Synthesis of Dysiherbols A, C, and D

S Hu, Y Tang - Journal of the American Chemical Society, 2022 - ACS Publications
Herein, we report the enantioselective total synthesis of dysiherbols A, C, and D, a unique
group of 6/6/5/6/6 pentacyclic quinone/hydroquinone sesquiterpenes, featuring a photo …

Divergent total synthesis of the revised structures of marine anti-cancer meroterpenoids (+)-dysiherbols A–E

C Chong, L Chang, I Grimm, Q Zhang, Y Kuang… - Chemical …, 2023 - pubs.rsc.org
We report here a concise and divergent enantioselective total synthesis of the revised
structures of marine anti-cancer sesquiterpene hydroquinone meroterpenoids (+) …

Enantioselective Total Synthesis of (−)‐Hosieine A

J Ouyang, R Yan, X Mi, R Hong - … Chemie International Edition, 2015 - Wiley Online Library
The first total synthesis of (−)‐hosieine A was accomplished and features an unprecedented
nitroso–ene cyclization to construct the 2‐azabicyclo [3.2. 1] octane ring system. Phosphine …