Alleman C, Gadais C, Legentil L, Poree F
Beilstein J Org Chem. 2023; 19:245-281.
PMID: 36895430
PMC: 9989678.
DOI: 10.3762/bjoc.19.23.
Indu S, Kaliappan K
RSC Adv. 2022; 8(38):21292-21305.
PMID: 35557999
PMC: 9088519.
DOI: 10.1039/c8ra03338b.
Zheng H, Wang R, Wang K, Wherritt D, Arman H, Doyle M
Chem Sci. 2021; 12(13):4819-4824.
PMID: 34168758
PMC: 8179600.
DOI: 10.1039/d1sc00158b.
Santalla H, Gandara Z, Gomez-Bouzo U, Gomez G, Fall Y
ACS Omega. 2020; 5(40):26049-26055.
PMID: 33073131
PMC: 7557988.
DOI: 10.1021/acsomega.0c03504.
Licsandru E, Gaysinski M, Mija A
Polymers (Basel). 2020; 12(7).
PMID: 32708731
PMC: 7408238.
DOI: 10.3390/polym12071583.
Utilization of the Thorpe-Ingold Effect in the Synthesis of Cyclooctanoid Ring Systems via Anionic 6-- Cyclization/Claisen Rearrangement Sequence.
DeLomba W, Stone E, Alley K, Iannarone V, Tarsis E, Ovaska S
J Org Chem. 2020; 85(15):9464-9474.
PMID: 32687712
PMC: 8588887.
DOI: 10.1021/acs.joc.0c01132.
Palladium-Catalyzed Enantioselective Alkenylation of Enelactams Using a Relay Heck Strategy.
Yuan Q, Sigman M
Chemistry. 2019; 25(46):10823-10827.
PMID: 31216370
PMC: 6731067.
DOI: 10.1002/chem.201902813.
Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin.
Krout M, Henry C, Jensen T, Wu K, Virgil S, Stoltz B
J Org Chem. 2018; 83(13):6995-7009.
PMID: 29298482
PMC: 6035096.
DOI: 10.1021/acs.joc.7b02972.
Selective Synthesis of Cyclooctanoids by Radical Cyclization of Seven-Membered Lactones: Neutron Diffraction Study of the Stereoselective Deuteration of a Chiral Organosamarium Intermediate.
Just-Baringo X, Clark J, Gutmann M, Procter D
Angew Chem Int Ed Engl. 2016; 55(40):12499-502.
PMID: 27600354
PMC: 5113801.
DOI: 10.1002/anie.201606792.
Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade.
Brill Z, Grover H, Maimone T
Science. 2016; 352(6289):1078-82.
PMID: 27230373
PMC: 5319821.
DOI: 10.1126/science.aaf6742.
Stereoselective Synthesis of Substituted Oxocene Cores by Lewis Acid Promoted Cyclization.
Ghosh A, Tomaine A, Cantwell K
Org Lett. 2016; 18(3):396-9.
PMID: 26829580
PMC: 5317094.
DOI: 10.1021/acs.orglett.5b03411.
Facile Access to Cyclooctanoid Ring Systems via Microwave-Assisted Tandem 6-exo dig Cyclization-Rearrangement Sequence.
Feldman A, Ovaska S, Ovaska T
Tetrahedron. 2014; 70(27-28):4147-4155.
PMID: 24994941
PMC: 4074778.
DOI: 10.1016/j.tet.2014.02.089.
A [4 + 4] annulation strategy for the synthesis of eight-membered carbocycles based on intramolecular cycloadditions of conjugated enynes.
Robinson J, Tlais S, Fong J, Danheiser R
Tetrahedron. 2012; 67(51):9890-9898.
PMID: 22267878
PMC: 3260789.
DOI: 10.1016/j.tet.2011.09.031.
Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-induced cyclizations.
Saadi J, Brudgam I, Reissig H
Beilstein J Org Chem. 2011; 6:1229-45.
PMID: 21283559
PMC: 3028607.
DOI: 10.3762/bjoc.6.141.
Asymmetric synthesis of medium-sized rings by intramolecular Au(I)-catalyzed cyclopropanation.
Watson I, Ritter S, Toste F
J Am Chem Soc. 2009; 131(6):2056-7.
PMID: 19161306
PMC: 2662771.
DOI: 10.1021/ja8085005.
Studies towards the total synthesis of di- and sesterterpenes with dicyclopenta[a,d]cyclooctane skeletons. Three-component approach to the A/B rings building block.
Michalak K, Michalak M, Wicha J
Molecules. 2007; 10(9):1084-100.
PMID: 18007374
PMC: 6147619.
DOI: 10.3390/10091084.
Recent Developments in Rhodium-Catalyzed Allylic Substitution and Carbocyclization Reactions.
Evans P, Leahy D
Chemtracts. 2006; 16(9):567-578.
PMID: 17047733
PMC: 1615892.