Cross-coupling reactions using samarium (II) iodide

M Szostak, NJ Fazakerley, D Parmar… - Chemical …, 2014 - ACS Publications
Since its introduction to organic synthesis in 1977 by Kagan, 1, 2 samarium (II) iodide (SmI2,
Kagan's reagent) has gained the status of one of the most versatile single-electron transfer …

New developments of the principle of vinylogy as applied to π-extended enolate-type donor systems

C Curti, L Battistini, A Sartori, F Zanardi - Chemical reviews, 2020 - ACS Publications
The principle of vinylogy states that the electronic effects of a functional group in a molecule
are possibly transmitted to a distal position through interposed conjugated multiple bonds …

The impact of the Mukaiyama aldol reaction in total synthesis

SBJ Kan, KKH Ng, I Paterson - … Chemie International Edition, 2013 - Wiley Online Library
Four decades since Mukaiyama's first reports on the successful application of silicon and
boron enolates in directed aldol reactions, the ability of this highly controlled carbon–carbon …

Electrophilic Rearrangements of Chiral Amides: A Traceless Asymmetric α-Allylation

B Peng, D Geerdink, N Maulide - Journal of the American …, 2013 - ACS Publications
A one-pot protocol for the asymmetric α-allylation reaction is reported relying on a key
efficient asymmetric Claisen rearrangement, triggered by electrophilic activation of chiral …

Samarium (ii) iodide-mediated reactions applied to natural product total synthesis

MM Heravi, A Nazari - RSC advances, 2022 - pubs.rsc.org
Natural product synthesis remains a field in which new synthetic methods and reagents are
continually being evaluated. Due to the demanding structures and complex functionality of …

Stereoconfining macrocyclizations in the total synthesis of natural products

K Zheng, R Hong - Natural Product Reports, 2019 - pubs.rsc.org
Covering: selected examples in the past three decades (up to 2018) The challenging
structures and often potent biological activities of naturally occurring macrocycles have …

[HTML][HTML] Recent developments in the asymmetric Reformatsky-type reaction

H Pellissier - Beilstein Journal of Organic Chemistry, 2018 - beilstein-journals.org
This review collects the most important developments in asymmetric Reformatsky-type
reactions published since the beginning of 2013, including both diastereoselective …

Progress in catalytic asymmetric α-functionalization of vinylogous nucleophilic species

ZH Wang, Y You, JQ Zhao, YP Zhang, JQ Yin… - Organic Chemistry …, 2023 - pubs.rsc.org
In conjugated π systems, π-extended enolates generated in situ from unsaturated
pronucleophiles through suitable HOMO-raising strategies tend to proceed via …

Scalable Total Syntheses of (±)-Catellatolactams A and B

H Yang, Y Zhang, W Chen, H Shi, L Huo, J Li, H Li… - Organic …, 2023 - ACS Publications
The first total syntheses of (±)-catellatolactams A and B, two novel ansamacrolactams, are
described in 5 and 8 steps, respectively. The strategy relies on an amidation reaction to …

[HTML][HTML] Absolute configuration reassignment of natural products: an overview of the last decade

ANL Batista, BRP Angrisani, MED Lima… - Journal of the Brazilian …, 2021 - SciELO Brasil
The assignment of absolute configuration (AC) is a crucial step in the structural
characterization of natural products, especially for those subjected to biological assays …