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For: Lee HM, Nieto-Oberhuber C, Shair MD. Enantioselective synthesis of (+)-cortistatin a, a potent and selective inhibitor of endothelial cell proliferation. J Am Chem Soc 2008;130:16864-6. [PMID: 19053422 DOI: 10.1021/ja8071918] [Cited by in Crossref: 137] [Cited by in F6Publishing: 99] [Article Influence: 10.5] [Reference Citation Analysis]
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3 Chen Y, Guo L, Xu J. Synthesis of the tricyclic skeleton of Daphniphyllum alkaloids daphnimacropodines. Tetrahedron Letters 2021;71:153030. [DOI: 10.1016/j.tetlet.2021.153030] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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11 Chen W, Wang L, Li Y. C-H Functionalization of Amino Alcohols by Osmium Tetroxide/NMO or TPAP/NMO: Protecting Group-Free Synthesis of Indolizidines (-)-223AB and 3- epi -(-)-223AB: C-H Functionalization of Amino Alcohols by Osmium Tetroxide/NMO or TPAP/NMO: Protecting Group-Free Synthesis of Indolizidines (-)-223AB and 3-epi-(-)-. Eur J Org Chem 2020;2020:103-7. [DOI: 10.1002/ejoc.201901494] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Wang Y, Ju W, Tian H, Sun S, Li X, Tian W, Gui J. Facile Access to Bridged Ring Systems via Point-to-Planar Chirality Transfer: Unified Synthesis of Ten Cyclocitrinols. J Am Chem Soc 2019;141:5021-33. [PMID: 30827095 DOI: 10.1021/jacs.9b00925] [Cited by in Crossref: 15] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
13 Bao W, Tao Y, Cheng J, Huang J, Cao J, Zhang M, Ye W, Wang B, Li Y, Zhu L, Lee CS. In(OTf)3-Catalyzed Cascade Cyclization for Construction of Oxatricyclic Compounds. Org Lett 2018;20:7912-5. [PMID: 30543298 DOI: 10.1021/acs.orglett.8b03461] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
14 Tang J, Chen EY. Effects of Chain Ends on Thermal and Mechanical Properties and Recyclability of Poly( γ ‐butyrolactone). J Polym Sci Part A: Polym Chem 2018;56:2271-9. [DOI: 10.1002/pola.29180] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
15 Sanz-Marco A, Martinez-Erro S, Martín-Matute B. Selective Synthesis of Unsymmetrical Aliphatic Acyloins through Oxidation of Iridium Enolates. Chemistry 2018;24:11564-7. [PMID: 29928782 DOI: 10.1002/chem.201803117] [Cited by in Crossref: 5] [Article Influence: 1.3] [Reference Citation Analysis]
16 Lu Z, Zhang X, Guo Z, Chen Y, Mu T, Li A. Total Synthesis of Aplysiasecosterol A. J Am Chem Soc 2018;140:9211-8. [PMID: 29939021 DOI: 10.1021/jacs.8b05070] [Cited by in Crossref: 45] [Cited by in F6Publishing: 30] [Article Influence: 11.3] [Reference Citation Analysis]
17 Hatcher JM, Wang ES, Johannessen L, Kwiatkowski N, Sim T, Gray NS. Development of Highly Potent and Selective Steroidal Inhibitors and Degraders of CDK8. ACS Med Chem Lett 2018;9:540-5. [PMID: 29937979 DOI: 10.1021/acsmedchemlett.8b00011] [Cited by in Crossref: 48] [Cited by in F6Publishing: 46] [Article Influence: 12.0] [Reference Citation Analysis]
18 Chandrashekhar R, Vemulapalli SPB, Sridhar B, Subba Reddy BV. Stereoselective Construction of Spiro-Indolenine Frameworks through a Prins/Friedel-Crafts Cyclization Cascade Reaction: Stereoselective Construction of Spiro-Indolenine Frameworks through a Prins/Friedel-Crafts Cyclization Cascade Reaction. Eur J Org Chem 2018;2018:1693-8. [DOI: 10.1002/ejoc.201701812] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
19 Faisal M, Shahzad D, Larik FA, Dar P. Synthetic approaches to access acortatarins, shensongines and pollenopyrroside; potent antioxidative spiro-alkaloids with a naturally rare morpholine moiety. Fitoterapia 2018;129:366-82. [PMID: 29617626 DOI: 10.1016/j.fitote.2018.03.014] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
20 Bhagwat AS, Lu B, Vakoc CR. Enhancer dysfunction in leukemia. Blood 2018;131:1795-804. [PMID: 29439951 DOI: 10.1182/blood-2017-11-737379] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
21 Liu JJ, Huang HY, Cheng L, Liu Q, Wang D, Liu L. A catalyst-free intermolecular trans-iodoalkylation of alkynes. Org Biomol Chem 2018;16:899-903. [PMID: 29350733 DOI: 10.1039/c7ob03159a] [Cited by in Crossref: 10] [Article Influence: 2.5] [Reference Citation Analysis]
22 Liu L, Cheng HL, Ma WQ, Hou SH, Tu YQ, Zhang FM, Zhang XM, Wang SH. Improved synthesis of 8-oxabicyclo[3.2.1]octanes via tandem C-H oxidation/oxa-[3,3] Cope rearrangement/aldol cyclization. Chem Commun (Camb) 2018;54:196-9. [PMID: 29226934 DOI: 10.1039/c7cc08511g] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
23 Someswarao B, P. RK, Reddy BJM, B. S, B. VSR. Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems. Org Chem Front 2018;5:1320-4. [DOI: 10.1039/c7qo01164d] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 1.8] [Reference Citation Analysis]
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26 Czerwiński P, Michalak M. NHC-Cu(I)-Catalyzed Friedländer-Type Annulation of Fluorinated o-Aminophenones with Alkynes on Water: Competitive Base-Catalyzed Dibenzo[b,f][1,5]diazocine Formation. J Org Chem 2017;82:7980-97. [PMID: 28686022 DOI: 10.1021/acs.joc.7b01235] [Cited by in Crossref: 15] [Article Influence: 3.0] [Reference Citation Analysis]
27 Armaly AM, Bar S, Schindler CS. Aluminum Chloride-Mediated Dieckmann Cyclization for the Synthesis of Cyclic 2-Alkyl-1,3-alkanediones: One-Step Synthesis of the Chiloglottones. Org Lett 2017;19:3958-61. [DOI: 10.1021/acs.orglett.7b01622] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
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29 Zweig JE, Kim DE, Newhouse TR. Methods Utilizing First-Row Transition Metals in Natural Product Total Synthesis. Chem Rev 2017;117:11680-752. [PMID: 28525261 DOI: 10.1021/acs.chemrev.6b00833] [Cited by in Crossref: 103] [Cited by in F6Publishing: 68] [Article Influence: 20.6] [Reference Citation Analysis]
30 Zhurakovskyi O, Ellis SR, Thompson AL, Robertson J. Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland–Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl. Org Lett 2017;19:2174-7. [DOI: 10.1021/acs.orglett.7b00834] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.6] [Reference Citation Analysis]
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32 Kotoku N, Ito A, Shibuya S, Mizuno K, Takeshima A, Nogata M, Kobayashi M. Short-step synthesis and structure-activity relationship of cortistatin A analogs. Tetrahedron 2017;73:1342-9. [DOI: 10.1016/j.tet.2017.01.042] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
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34 Hu Z, Dong J, Men Y, Li Y, Xu X. Organocatalyzed aerobic oxidative Robinson-type annulation of 2-isocyanochalcones: expedient synthesis of phenanthridines. Chem Commun 2017;53:1739-42. [DOI: 10.1039/c6cc09430a] [Cited by in Crossref: 30] [Article Influence: 6.0] [Reference Citation Analysis]
35 Li H, Chen Q, Lu Z, Li A. Total Syntheses of Aflavazole and 14-Hydroxyaflavinine. J Am Chem Soc 2016;138:15555-8. [DOI: 10.1021/jacs.6b10880] [Cited by in Crossref: 48] [Cited by in F6Publishing: 35] [Article Influence: 8.0] [Reference Citation Analysis]
36 Gao AX, Hamada T, Snyder SA. The Enantioselective Total Synthesis of Exochomine. Angew Chem Int Ed 2016;55:10301-6. [DOI: 10.1002/anie.201604744] [Cited by in Crossref: 21] [Cited by in F6Publishing: 15] [Article Influence: 3.5] [Reference Citation Analysis]
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38 Aquino C, Greszler SN, Micalizio GC. Synthesis of the Cortistatin Pentacyclic Core by Alkoxide-Directed Metallacycle-Mediated Annulative Cross-Coupling. Org Lett 2016;18:2624-7. [PMID: 27193994 DOI: 10.1021/acs.orglett.6b01048] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
39 Zhang J, You L, Wang Y, Li Y, Liang X, Zhang B, Yang S, Su Q, Chen J, Yang Z. Asymmetric Total Synthesis of Propindilactone G, Part 2: Enantioselective Construction of the Fully Functionalized BCDE Ring System. Chem Asian J 2016;11:1414-24. [DOI: 10.1002/asia.201600130] [Cited by in Crossref: 17] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
40 Reddy BS, Swathi V, Bhadra MP, Raju MK, Kunwar A. Tandem vinylcyclopropane ring opening/Prins cyclization for the synthesis of 2,3-disubstituted tetrahydropyrans. Tetrahedron Letters 2016;57:1889-91. [DOI: 10.1016/j.tetlet.2016.03.062] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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43 Peng C, Hong B, Raja A, Chang C, Lee G. Constructing densely functionalized Hajos–Parrish-type ketones with six contiguous stereogenic centers and two quaternary carbons in a formal [2 + 2 + 2] cycloaddition cascade. RSC Adv 2016;6:95314-9. [DOI: 10.1039/c6ra22430j] [Cited by in Crossref: 4] [Article Influence: 0.7] [Reference Citation Analysis]
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47 Reddy BVS, Reddy GN, Reddy MR, Lakshmi JK, Jagadeesh B, Sridhar B. Prins-Driven Friedel-Crafts Reaction for the Stereoselective Synthesis of Hexahydroindeno[2,1- c ]pyran Derivatives. Asian J Org Chem 2015;4:1266-72. [DOI: 10.1002/ajoc.201500218] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
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49 Reddy BV, Someswarao B, Prudhviraju N, Reddy BJ, Sridhar B, Kumar SK. An iodine catalyzed metal free domino process for the stereoselective synthesis of oxygen bridged bicyclic ethers. Org Biomol Chem 2015;13:6737-41. [PMID: 25994362 DOI: 10.1039/c5ob00518c] [Cited by in Crossref: 3] [Article Influence: 0.4] [Reference Citation Analysis]
50 Subba Reddy BV, Prudhvi Raju N, Someswarao B, Mohan Reddy BJ, Sridhar B, Marumudi K, Kunwar AC. A novel domino cyclization for the stereoselective synthesis of indeno[2,1-c]pyran and cyclopenta[c]pyran derivatives. Org Biomol Chem 2015;13:4733-6. [PMID: 25804904 DOI: 10.1039/c5ob00376h] [Cited by in Crossref: 6] [Article Influence: 0.9] [Reference Citation Analysis]
51 Reddy BVS, Reddy MR, Reddy SG, Sridhar B, Kumar SK. Tandem Prins Cyclization for the Stereoselective Synthesis of the 4,5-Diaryl-hexahydropyrano[3,4- c ]chromene Skeleton of Calyxins I and J: Tandem Prins Cyclization for the Synthesis of Calyxin Analogues. Eur J Org Chem 2015;2015:3103-8. [DOI: 10.1002/ejoc.201500117] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
52 Reddy BVS, Yarlagadda S, Reddy CR, Reddy MR, Sridhar B, Satyanarayana D, Jagadeesh B. Tandem Prins Strategy for the Synthesis of Spiropyrrolidine and Spiropiperidine Derivatives: Synthesis of Heterocyclic Spiro Compounds. Eur J Org Chem 2015;2015:3076-85. [DOI: 10.1002/ejoc.201500215] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
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58 Subba Reddy BV, Gopal Reddy S, Ramana Reddy M, Pal Bhadra M, Sarma AVS. Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds. Org Biomol Chem 2014;12:7257. [DOI: 10.1039/c4ob01188k] [Cited by in Crossref: 13] [Article Influence: 1.6] [Reference Citation Analysis]
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60 Reddy BVS, Kumar H, Reddy PS, Singarapu KK. Prins Spirocyclization for the Synthesis of Spiro[isobenzofuran-pyran] Derivatives: Prins Spirocyclization. Eur J Org Chem 2014;2014:4234-8. [DOI: 10.1002/ejoc.201402157] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
61 Subba Reddy BV, Medaboina D, Sridhar B, Singarapu KK. Prins Cascade Cyclization for the Synthesis of 1,9-Dioxa-4-azaspiro[5.5]undecane Derivatives. J Org Chem 2014;79:2289-95. [DOI: 10.1021/jo4027534] [Cited by in Crossref: 24] [Cited by in F6Publishing: 11] [Article Influence: 3.0] [Reference Citation Analysis]
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