Liu M, Ohashi M, Zhou Q, Sanders J, McCauley E, Crews P
Angew Chem Int Ed Engl. 2023; 62(40):e202311266.
PMID: 37589717
PMC: 10868402.
DOI: 10.1002/anie.202311266.
Zhang Z, Liu L, Liu Y, Lin J, Lu X, Ye L
Chem Sci. 2023; 14(22):5918-5924.
PMID: 37293635
PMC: 10246658.
DOI: 10.1039/d3sc01880f.
Sabat N, Zhou W, Gandon V, Guinchard X, Vincent G
Angew Chem Int Ed Engl. 2022; 61(30):e202204400.
PMID: 35570713
PMC: 9401073.
DOI: 10.1002/anie.202204400.
Silva R, da Silva M, Jacomini A, Moura S, Back D, Basso E
RSC Adv. 2022; 8(9):4773-4778.
PMID: 35539545
PMC: 9077875.
DOI: 10.1039/c7ra13343j.
Chernowsky C, Chmiel A, Wickens Z
Angew Chem Int Ed Engl. 2021; 60(39):21418-21425.
PMID: 34288312
PMC: 8440429.
DOI: 10.1002/anie.202107169.
Unconventional Macrocyclizations in Natural Product Synthesis.
Saridakis I, Kaiser D, Maulide N
ACS Cent Sci. 2020; 6(11):1869-1889.
PMID: 33274267
PMC: 7706100.
DOI: 10.1021/acscentsci.0c00599.
The quest for supernatural products: the impact of total synthesis in complex natural products medicinal chemistry.
Wu Z, Boger D
Nat Prod Rep. 2020; 37(11):1511-1531.
PMID: 33169762
PMC: 7678878.
DOI: 10.1039/d0np00060d.
Natural Products in the "Marketplace": Interfacing Synthesis and Biology.
Huffman B, Shenvi R
J Am Chem Soc. 2019; 141(8):3332-3346.
PMID: 30682249
PMC: 6446556.
DOI: 10.1021/jacs.8b11297.
Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.
Susick R, Morrill L, Picazo E, Garg N
Synlett. 2018; 28(1):1-11.
PMID: 29540961
PMC: 5846481.
DOI: 10.1055/s-0036-1588372.
External oxidant-free electrooxidative [3 + 2] annulation between phenol and indole derivatives.
Liu K, Tang S, Huang P, Lei A
Nat Commun. 2017; 8(1):775.
PMID: 28974679
PMC: 5626759.
DOI: 10.1038/s41467-017-00873-1.
Oxidative dehydrogenation of C-C and C-N bonds: A convenient approach to access diverse (dihydro)heteroaromatic compounds.
Hati S, Holzgrabe U, Sen S
Beilstein J Org Chem. 2017; 13:1670-1692.
PMID: 28904611
PMC: 5564259.
DOI: 10.3762/bjoc.13.162.
Unified biomimetic assembly of voacalgine A and bipleiophylline via divergent oxidative couplings.
Lachkar D, Denizot N, Bernadat G, Ahamada K, Beniddir M, Dumontet V
Nat Chem. 2017; 9(8):793-798.
PMID: 28754932
DOI: 10.1038/nchem.2735.
Synthesis of 2-oxindoles via 'transition-metal-free' intramolecular dehydrogenative coupling (IDC) of sp(2) C-H and sp(3) C-H bonds.
Kumar N, Ghosh S, Bhunia S, Bisai A
Beilstein J Org Chem. 2016; 12:1153-1169.
PMID: 27559367
PMC: 4979638.
DOI: 10.3762/bjoc.12.111.
Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable Method.
Horn E, Rosen B, Baran P
ACS Cent Sci. 2016; 2(5):302-8.
PMID: 27280164
PMC: 4882743.
DOI: 10.1021/acscentsci.6b00091.
Natural product synthesis at the interface of chemistry and biology.
Hong J
Chemistry. 2014; 20(33):10204-12.
PMID: 25043880
PMC: 4167019.
DOI: 10.1002/chem.201402804.
Total synthesis of diazonamide A.
Knowles R, Carpenter J, Blakey S, Kayano A, Mangion I, Sinz C
Chem Sci. 2012; 2011(2):308-311.
PMID: 22860227
PMC: 3408608.
DOI: 10.1039/C0SC00577K.
Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.
Nicolaou K, Hale C, Nilewski C, Ioannidou H
Chem Soc Rev. 2012; 41(15):5185-238.
PMID: 22743704
PMC: 3426871.
DOI: 10.1039/c2cs35116a.
Alpha-arylation of 3-aryloxindoles.
Mai C, Sammons M, Sammakia T
Org Lett. 2010; 12(10):2306-9.
PMID: 20426400
PMC: 2896240.
DOI: 10.1021/ol100666v.
A concise formal synthesis of diazonamide A by the stereoselective construction of the C10 quaternary center.
Mai C, Sammons M, Sammakia T
Angew Chem Int Ed Engl. 2010; 49(13):2397-400.
PMID: 20191642
PMC: 3540747.
DOI: 10.1002/anie.200906318.
Total synthesis of atrochamins F, H, I, and J through cascade reactions.
Nicolaou K, Lister T, Denton R, Gelin C
Tetrahedron. 2009; 64(21):4736-4757.
PMID: 19461992
PMC: 2597834.
DOI: 10.1016/j.tet.2008.02.108.
