Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

M Ishikura, T Abe, T Choshi, S Hibino - Natural product reports, 2015 - pubs.rsc.org
Covering: 2012 to 2013. Previous review: Nat. Prod. Rep., 2013, 30, 694–752 This review
covers the literature on simple indole alkaloids and those with a nonrearranged …

From synthetic control to natural products: a focus on N‐heterocycles

C Prandi, EG Occhiato - Pest management science, 2019 - Wiley Online Library
Natural products containing a N‐heterocycle motif are widespread in nature and medicinal
plants, in particular, have proved to be a source of almost unlimited N‐derived structures …

Catalytic asymmetric indolization by a desymmetrizing [3+ 2] annulation strategy

C Wu, Z Chang, C Peng, C Bai, J Xing, X Dou - Chemical Science, 2023 - pubs.rsc.org
A new catalytic asymmetric indolization reaction by a desymmetrizing [3+ 2] annulation
strategy is developed. The reaction proceeds via a rhodium-catalyzed enantioposition …

Gold-catalyzed skeletal rearrangement of alkenes: regioselective synthesis of skeletally diverse tricyclic heterocycles and mechanistic investigations

XY Qin, FT Meng, M Wang, SJ Tu, WJ Hao… - ACS …, 2021 - ACS Publications
Transition metal-catalyzed skeletal rearrangement reactions have rapid advances in organic
community. Their development benefits synthetic methodologies by providing versatile and …

Gold (I)‐Catalyzed 1, 2‐Acyloxy Migration/[3+ 2] Cycloaddition of 1, 6‐Diynes with an Ynamide Propargyl Ester Moiety: Highly Efficient Synthesis of Functionalized …

J Liu, M Chen, L Zhang, Y Liu - Chemistry–A European Journal, 2015 - Wiley Online Library
A gold‐catalyzed cycloisomerization of 1, 6‐diynes containing an ynamide propargyl ester
or carbonate moiety has been developed that provides an attractive route to a diverse …

Synthesis of Cyclopenta[b]indoles via Sc(III)-Catalyzed Annulation of Vinyl Diazoacetates with Indole-Derived Unsaturated Imines

Q Jiang, T Yang, Q Li, GM Liang, Y Liu, CY He… - Organic …, 2023 - ACS Publications
A Lewis acid Sc (OTf) 3-catalyzed annulation reaction of vinyl diazoacetates with in situ
formed α, β-unsaturated imines for the preparation of indole-fused tricyclic rings has been …

Highly regio-and enantioselective formal [3+ 2]-annulation of indoles with electrophilic enol carbene intermediates

C Jing, QQ Cheng, Y Deng, H Arman, MP Doyle - Organic letters, 2016 - ACS Publications
Chiral cyclopentane-fused indolines are synthesized with high regio-and enantiocontrol by
formal [3+ 2]-annulation reactions of indoles and electrophilic enol carbenes. High …

Iron-Mediated Hydrogen Atom Transfer Radical Cyclization of Alkenyl Indoles and Pyrroles Gives Their Fused Derivatives: Total Synthesis of Bruceolline E and H

SJ Gharpure, RS Chavan, SR Narang - Organic Letters, 2024 - ACS Publications
The iron-mediated hydrogen atom transfer (HAT) reaction is efficaciously employed for the
synthesis of dihydropyrroloindoles and dihydropyrrolizines via 5-exo-trig radical cyclization …

Catalytic enantioselective desymmetrizing Fischer indolization through dynamic kinetic resolution

B Ghosh, R Balhara, G Jindal… - Angewandte Chemie …, 2021 - Wiley Online Library
The first catalytic enantioselective Fischer indolization of prochiral diketones containing
enantiotopic carbonyl groups is developed and shown to proceed through dynamic kinetic …

Protecting group-free syntheses of natural products and biologically active compounds

RN Saicic - Tetrahedron, 2014 - Elsevier
At the beginning of the 21st century, the art and science of organic synthesis face the
challenge of optimizing efficiency. One may assert that the need for efficiency has always …