Tetracyclic diterpenoid synthesis facilitated by ODI-cascade approaches to bicyclo [3.2. 1] octane skeletons

K Gao, J Hu, H Ding - Accounts of Chemical Research, 2021 - ACS Publications
Conspectus Tetracyclic diterpenoids (C20) mainly refer to the plant terpenoids bearing
biogenetically related carbon skeletons derived from copalyl diphosphates (ent-CPP and …

Total syntheses of trichorabdal A and maoecrystal Z

Z Lv, B Chen, C Zhang, G Liang - Chemistry–A European …, 2018 - Wiley Online Library
This work reports the total syntheses of Isodon diterpenes trichorabdal A and maoecrystal Z
via a common bicyclo [3.2. 1] octane intermediate, which chemically bridges the two distinct …

Type II intramolecular [5+ 2] cycloaddition: facile synthesis of highly functionalized bridged ring systems

G Mei, X Liu, C Qiao, W Chen… - Angewandte Chemie …, 2015 - Wiley Online Library
A type II intramolecular oxidopyrylium‐mediated [5+ 2] cycloaddition reaction allows the
efficient and diastereoselective formation of various highly functionalized and synthetically …

Total Syntheses of Rhodomolleins XX and XXII: A Reductive Epoxide‐Opening/Beckwith–Dowd Approach

K Yu, ZN Yang, CH Liu, SQ Wu, X Hong… - Angewandte Chemie …, 2019 - Wiley Online Library
A new TiIII‐mediated reductive epoxide‐opening/Beckwith–Dowd rearrangement process
efficiently assembles the bicyclo [3.2. 1] octane framework of highly oxidized grayanane …

A divergent [5+ 2] cascade approach to bicyclo [3.2. 1] octanes: facile synthesis of ent-kaurene and cedrene-type skeletons

C He, Z Bai, J Hu, B Wang, H Xie, L Yu… - Chemical …, 2017 - pubs.rsc.org
A solvent-dependent oxidative dearomatization-induced divergent [5+ 2] cascade approach
to bicyclo [3.2. 1] octanes was described. This novel protocol enables a facile synthesis of a …

Recent synthetic studies towards natural products via [5+ 2] cycloaddition reactions

X Liu, YJ Hu, JH Fan, J Zhao, S Li, CC Li - Organic Chemistry Frontiers, 2018 - pubs.rsc.org
[5+ 2] Cycloaddition reactions have attracted increasing attention from the chemistry
community owing to their utility in the field of natural product synthesis. Recently, a number …

Formal syntheses of (±)-Asterisca-3 (15), 6-diene and (±)-Pentalenene using Rh (I)-catalyzed [(5+ 2)+ 1] cycloaddition

X Fan, LG Zhuo, YQ Tu, ZX Yu - Tetrahedron, 2009 - Elsevier
Efficient formal syntheses of (±)-Asterisca-3 (15), 6-diene, a natural product with a bicyclo
[6.3. 0] undecane skeleton, and (±)-Pentalenene, a natural product with a tricyclo [6.3. 0.04 …

Expeditious Divergent Synthetic Approach to Polycyclic Terpene‐Like Molecules

T Boddaert, Y Coquerel, J Rodriguez - Chemistry–A European Journal, 2011 - infona.pl
The domino effect: The combination of two multiple bond‐forming transformations; a
consecutive Wolff rearrangement/acylketene‐trapping cross metathesis reaction and a …

Straightforward access to the [3.2. 2] nonatriene structural framework via intramolecular cyclopropenation/Buchner reaction/Cope rearrangement cascade

X Xu, X Wang, PY Zavalij, MP Doyle - Organic letters, 2015 - ACS Publications
A one-pot cascade process of benzyl enoldiazoacatates, initiated by dirhodium (II)-catalyzed
intramolecular cyclopropene formation, occurs via a subsequent Buchner reaction and Cope …

Application of (4+ 3) cycloaddition strategies in the synthesis of natural products

Z Yin, Y He, P Chiu - Chemical Society Reviews, 2018 - pubs.rsc.org
(4+ 3) Cycloadditions have been widely applied in synthesis, and in this review article, we
summarize some of the more recent applications, including formal (4+ 3) cycloadditions, in …