Simple indole alkaloids and those with a non-rearranged monoterpenoid unit

M Ishikura, T Abe, T Choshi, S Hibino - Natural Product Reports, 2013 - pubs.rsc.org
Covering: 2010–2011. Previous review: Nat. Prod. Rep. 2010, 27, 1630–1680This review
covers the literature on simple indole alkaloids and those with a non-rearranged …

Stereodivergent Construction of Contiguous Quaternary Carbon Centers Enabled by Asymmetric Catalysis

J Huo, X Li, Q Chen, P Gao, Y Hou, P Lei, H Zou… - ACS …, 2023 - ACS Publications
Herein, we report the discovery of the catalytic asymmetric conjugated addition of
allylstannanes to indol-2-ones promoted by Ni (II)/chiral N, N′-dioxide. This method …

[HTML][HTML] Total synthesis of (−)-penicimutanin a and related congeners

H Yu, Y Zong, T Xu - Chemical Science, 2020 - pubs.rsc.org
The first total synthesis of penicimutanin A (1) was achieved within 10 steps (LLS). Key
innovations in this synthesis consist of (1) a highly efficient electro-oxidative …

Catalytic Asymmetric Reverse Prenylation of Indol-2-one Enabled a Synthesis of (−)-Debromoflustramine A

Y Hou, J Huo, R Li, J Hou, P Lei, H Wei, W Xie - Organic Letters, 2023 - ACS Publications
A catalytic asymmetric nucleophilic reverse prenylation of indol-2-ones in situ generated
from 3-bromooxindoles with prenyltributylstannane promoted by Ni (II)/chiral N, N′-dioxide …

Enantioselective construction of spirocyclic oxindole derivatives with multiple stereocenters via an organocatalytic Michael/aldol/hemiacetalization cascade reaction

L Zhu, Q Chen, D Shen, W Zhang, C Shen, X Zeng… - Organic …, 2016 - ACS Publications
An efficient organocatalytic Michael/aldol/hemiacetalization cascade reaction for
construction of enantioenriched spirocyclic oxindoles fused with tetrahydropyrane has been …

PhI (OAc) 2/NaX-mediated halogenation providing access to valuable synthons 3-haloindole derivatives

V Himabindu, SP Parvathaneni, VJ Rao - New Journal of Chemistry, 2018 - pubs.rsc.org
This paper describes a mild phenyliodine diacetate mediated method for selective
chlorination, bromination, and iodination of indole C–H bonds using sodium halide as a …

Pd/Cu cocatalyzed oxidative tandem C–H aminocarbonylation and dehydrogenation of tryptamines: synthesis of carbolinones

H Han, SD Yang, JB Xia - The Journal of Organic Chemistry, 2019 - ACS Publications
The Pd/Cu cocatalyzed oxidative tandem C–H aminocarbonylation and dehydrogenation
was developed, affording carbolinones with molecular oxygen as the terminal oxidant …

Indole-Catalyzed Bromolactonization in Lipophilic Solvent: A Solid–Liquid Phase Transfer Approach

T Chen, TJY Foo, YY Yeung - ACS Catalysis, 2015 - ACS Publications
We have developed a novel indole-catalyzed bromolactonization of olefinic acids. The
reaction could be conducted in lipophilic solvent through a solid–liquid phase transfer …

Palladium-Catalyzed Synthesis of N-tert-Prenylindoles

KF Johnson, R Van Zeeland, LM Stanley - Organic letters, 2013 - ACS Publications
Palladium-Catalyzed Synthesis of N-tert-Prenylindoles | Organic Letters ACS ACS Publications
C&EN CAS Find my institution Log In Organic Letters ACS Publications. Most Trusted. Most …

Stereoselective synthesis of spirocyclic oxindoles based on a one-pot Ullmann coupling/Claisen rearrangement and its application to the synthesis of a …

H Miyamoto, T Hirano, Y Okawa, A Nakazaki… - Tetrahedron, 2013 - Elsevier
An efficient and convenient approach to the synthesis of spirocyclic oxindoles from
iodoindoles has been developed. The most striking feature of this approach is that the …