BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Yoritate M, Takahashi Y, Tajima H, Ogihara C, Yokoyama T, Soda Y, Oishi T, Sato T, Chida N. Unified Total Synthesis of Stemoamide-Type Alkaloids by Chemoselective Assembly of Five-Membered Building Blocks. J Am Chem Soc 2017;139:18386-91. [PMID: 29179540 DOI: 10.1021/jacs.7b10944] [Cited by in Crossref: 69] [Cited by in F6Publishing: 74] [Article Influence: 13.8] [Reference Citation Analysis]
Number Citing Articles
1 Chen H, Wu Z, Shao D, Huang P. Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides. Sci Adv 2022;8. [DOI: 10.1126/sciadv.ade3431] [Reference Citation Analysis]
2 Liang YQ, Xu YX, Cai ZJ, Ji SJ. Visible-light photocatalytic radical addition-translocation-cyclization to construct sulfonyl-containing azacycles. Chem Commun (Camb) 2022. [PMID: 36000456 DOI: 10.1039/d2cc03799h] [Reference Citation Analysis]
3 Yoshii T, Mochida M, Kaizu K, Soda Y, Kanamori K, Nakanishi K, Sato T, Imai H, Citterio D, Hiruta Y. Amphiphilic Copolymer-Modified Eggshell-Based Column Packing Materials for the Preparative Separation of Basic Drugs. ACS Appl Polym Mater . [DOI: 10.1021/acsapm.2c00866] [Reference Citation Analysis]
4 Lang Q, Qian X, He X, Geng H, Zheng J, Huang P. A flexible enantioselective approach to 2,5-disubstituted cis-decahydroquinolines. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132935] [Reference Citation Analysis]
5 Chen J, Lim JW, Chiba S. Interception of enamine intermediates in reductive functionalization of lactams by sodium hydride: Synthesis of 2-cyano-3-iodo piperidines and pyrrolidines. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132779] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Shi T, Cao F, Chen J, Wang X, Yin G, Wang H, Wang Z. Total syntheses of seven stemoamide-type Stemona alkaloids. Org Chem Front 2022;9:771-4. [DOI: 10.1039/d1qo01578h] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Kuchkovska YO, Grygorenko OO. Azepines and Their Fused-Ring Derivatives. Comprehensive Heterocyclic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-818655-8.00073-1] [Reference Citation Analysis]
8 Deng Y, Liang X, Wei K, Yang YR. Ir-Catalyzed Asymmetric Total Syntheses of Bisdehydrotuberostemonine D, Putative Bisdehydrotuberostemonine E and Structural Revision of the Latter. J Am Chem Soc 2021;143:20622-7. [PMID: 34870982 DOI: 10.1021/jacs.1c11265] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
9 Olivier WJ, Smith JA, Bissember AC. Synthesis of Pyrrolidine- and γ-Lactam-Containing Natural Products and Related Compounds from Pyrrole Scaffolds. Chem Rec 2021. [PMID: 34862727 DOI: 10.1002/tcr.202100277] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
10 Li Z, Zhao F, Ou W, Huang P, Wang X. Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis. Angew Chem 2021;133:26808-13. [DOI: 10.1002/ange.202111029] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
11 Kim KE, Kim AN, McCormick CJ, Stoltz BM. Late-Stage Diversification: A Motivating Force in Organic Synthesis. J Am Chem Soc 2021;143:16890-901. [PMID: 34614361 DOI: 10.1021/jacs.1c08920] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 18.0] [Reference Citation Analysis]
12 Li Z, Zhao F, Ou W, Huang PQ, Wang X. Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis. Angew Chem Int Ed Engl 2021. [PMID: 34596947 DOI: 10.1002/anie.202111029] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 12.0] [Reference Citation Analysis]
13 Cao F, Gao W, Wang X, Zhang Z, Yin G, Wang Y, Li Z, Shi T, Hou Y, Chen J, Wang Z. Synthesis of the Proposed Structures of Parvistemoamide and Their Transformations to Stemoamide Derivatives. Org Lett 2021;23:6222-6. [PMID: 34369782 DOI: 10.1021/acs.orglett.1c01045] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
14 Matheau-Raven D, Dixon DJ. General α-Amino 1,3,4-Oxadiazole Synthesis via Late-Stage Reductive Functionalization of Tertiary Amides and Lactams*. Angew Chem Int Ed Engl 2021;60:19725-9. [PMID: 34191400 DOI: 10.1002/anie.202107536] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 14.0] [Reference Citation Analysis]
15 Matheau‐raven D, Dixon DJ. General α‐Amino 1,3,4‐Oxadiazole Synthesis via Late‐Stage Reductive Functionalization of Tertiary Amides and Lactams**. Angew Chem 2021;133:19877-81. [DOI: 10.1002/ange.202107536] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
16 Gabriel P, Almehmadi YA, Wong ZR, Dixon DJ. A General Iridium-Catalyzed Reductive Dienamine Synthesis Allows a Five-Step Synthesis of Catharanthine via the Elusive Dehydrosecodine. J Am Chem Soc 2021;143:10828-35. [PMID: 34254792 DOI: 10.1021/jacs.1c04980] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
17 Guo Z, Bao R, Li Y, Li Y, Zhang J, Tang Y. Tailored Synthesis of Skeletally Diverse Stemona Alkaloids through Chemoselective Dyotropic Rearrangements of β-Lactones. Angew Chem Int Ed Engl 2021;60:14545-53. [PMID: 33848039 DOI: 10.1002/anie.202102614] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 20.0] [Reference Citation Analysis]
18 Guo Z, Bao R, Li Y, Li Y, Zhang J, Tang Y. Tailored Synthesis of Skeletally Diverse Stemona Alkaloids through Chemoselective Dyotropic Rearrangements of β‐Lactones. Angew Chem 2021;133:14666-74. [DOI: 10.1002/ange.202102614] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
19 Wood MD, Klosowski DW, Martin SF. Tandem vinylogous Mannich and hetero Diels-Alder reactions: Concise total synthesis of (±)-Alstoscholarisine E. Tetrahedron 2021;89:132150. [DOI: 10.1016/j.tet.2021.132150] [Reference Citation Analysis]
20 Mkrtchyan S, Jakubczyk M, Lanka S, Pittelkow M, Iaroshenko VO. Cu-Catalyzed Arylation of Bromo-Difluoro-Acetamides by Aryl Boronic Acids, Aryl Trialkoxysilanes and Dimethyl-Aryl-Sulfonium Salts: New Entries to Aromatic Amides. Molecules 2021;26:2957. [PMID: 34065691 DOI: 10.3390/molecules26102957] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
21 Zheng Y, Yang HD, Wei K, Yang YR. Synthetic Studies toward Parvistemoline Using Asymmetric Ir/Amine-Catalyzed Allylation. J Org Chem 2021;86:6025-9. [PMID: 33769043 DOI: 10.1021/acs.joc.1c00390] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
22 Katahara S, Sugiyama Y, Yamane M, Komiya Y, Sato T, Chida N. Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via an Azomethine Ylide. Org Lett 2021;23:3058-63. [DOI: 10.1021/acs.orglett.1c00735] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 9.0] [Reference Citation Analysis]
23 Lin Y, He SF, Geng H, Xiao YC, Ji KL, Zheng JF, Huang PQ. Chemoselective Reactions of Isocyanates with Secondary Amides: One-Pot Construction of 2,3-Dialkyl-Substituted Quinazolinones. J Org Chem 2021;86:5345-53. [PMID: 33710879 DOI: 10.1021/acs.joc.0c02929] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
24 Yan F, Huang Z, Du C, Bai J, Li Y. Iron-catalyzed reductive strecker reaction. Journal of Catalysis 2021;395:188-94. [DOI: 10.1016/j.jcat.2021.01.003] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
25 Ong DY, Chen J, Chiba S. Reductive Functionalization of Carboxamides: A Recent Update. BCSJ 2020;93:1339-49. [DOI: 10.1246/bcsj.20200182] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
26 Uphade MB, Prasad KR. Formal total synthesis of (+)-stemoamide. Tetrahedron 2020;76:131623. [DOI: 10.1016/j.tet.2020.131623] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
27 Huang XZ, Gao LH, Huang PQ. Enantioselective total syntheses of (+)-stemofoline and three congeners based on a biogenetic hypothesis. Nat Commun 2020;11:5314. [PMID: 33082332 DOI: 10.1038/s41467-020-19163-4] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 9.0] [Reference Citation Analysis]
28 Soda Y, Sugiyama Y, Yoritate M, Tajima H, Shibuya K, Ogihara C, Oishi T, Sato T, Chida N. Unified Total Synthesis of Pentacyclic Stemoamide-type Alkaloids. Org Lett 2020;22:7502-7. [DOI: 10.1021/acs.orglett.0c02697] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 7.0] [Reference Citation Analysis]
29 Rogova T, Gabriel P, Zavitsanou S, Leitch JA, Duarte F, Dixon DJ. Reverse Polarity Reductive Functionalization of Tertiary Amides via a Dual Iridium-Catalyzed Hydrosilylation and Single Electron Transfer Strategy. ACS Catal 2020;10:11438-47. [DOI: 10.1021/acscatal.0c03089] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 11.5] [Reference Citation Analysis]
30 Panday SK. Pyroglutamic Acid and its Derivatives: The Privileged Precursors for the Asymmetric Synthesis of Bioactive Natural Products. MROC 2020;17:626-46. [DOI: 10.2174/1570193x16666190917142814] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
31 Matheau-raven D, Gabriel P, Leitch JA, Almehmadi YA, Yamazaki K, Dixon DJ. Catalytic Reductive Functionalization of Tertiary Amides using Vaska’s Complex: Synthesis of Complex Tertiary Amine Building Blocks and Natural Products. ACS Catal 2020;10:8880-97. [DOI: 10.1021/acscatal.0c02377] [Cited by in Crossref: 47] [Cited by in F6Publishing: 51] [Article Influence: 23.5] [Reference Citation Analysis]
32 Ham JS, Park B, Son M, Roque JB, Jurczyk J, Yeung CS, Baik MH, Sarpong R. C-H/C-C Functionalization Approach to N-Fused Heterocycles from Saturated Azacycles. J Am Chem Soc 2020;142:13041-50. [PMID: 32627545 DOI: 10.1021/jacs.0c04278] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 9.5] [Reference Citation Analysis]
33 Ong DY, Fan D, Dixon DJ, Chiba S. Transition-Metal-Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α-Branched Amine Synthesis. Angew Chem Int Ed Engl 2020;59:11903-7. [PMID: 32329555 DOI: 10.1002/anie.202004272] [Cited by in Crossref: 27] [Cited by in F6Publishing: 29] [Article Influence: 13.5] [Reference Citation Analysis]
34 Yin X, Ma K, Dong Y, Dai M. Pyrrole Strategy for the γ-Lactam-Containing Stemona Alkaloids: (±)Stemoamide, (±)Tuberostemoamide, and (±)Sessilifoliamide A. Org Lett 2020;22:5001-4. [PMID: 32551684 DOI: 10.1021/acs.orglett.0c01570] [Cited by in Crossref: 27] [Cited by in F6Publishing: 28] [Article Influence: 13.5] [Reference Citation Analysis]
35 Ong DY, Fan D, Dixon DJ, Chiba S. Transition‐Metal‐Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α‐Branched Amine Synthesis. Angew Chem 2020;132:12001-5. [DOI: 10.1002/ange.202004272] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 7.0] [Reference Citation Analysis]
36 Tahara A, Nagashima H. Recent topics of iridium-catalyzed hydrosilylation of tertiary amides to silylhemiaminals. Tetrahedron Letters 2020;61:151423. [DOI: 10.1016/j.tetlet.2019.151423] [Cited by in Crossref: 22] [Cited by in F6Publishing: 18] [Article Influence: 11.0] [Reference Citation Analysis]
37 Ou W, Lu G, An D, Han F, Huang P. Two-Step Catalytic Transformation of N -Benzyllactams to Alkaloids (±)-Solenopsin, (±)-Solenopsin A, and (+)-Julifloridine: Two-Step Catalytic Transformation of N -Benzyllactams to Alkaloids (±)-Solenopsin, (±)-Solenopsin A, and (+)-Julifloridine. Eur J Org Chem 2020;2020:52-6. [DOI: 10.1002/ejoc.201901752] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 4.7] [Reference Citation Analysis]
38 Wood MD, Klosowski DW, Martin SF. Stereoselective Total Synthesis of (±)-Alstoscholarisine E. Org Lett 2020;22:786-90. [DOI: 10.1021/acs.orglett.9b04093] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
39 Liu Y, Zhu C, Yu C, Wang A, Huang P. Tf 2 O-Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β-Enaminones: Tf 2 O-Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β-Enaminones. Eur J Org Chem 2019;2019:7169-74. [DOI: 10.1002/ejoc.201901354] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
40 Ou W, Huang P. Amides as surrogates of aldehydes for C-C bond formation: amide-based direct Knoevenagel-type condensation reaction and related reactions. Sci China Chem 2020;63:11-5. [DOI: 10.1007/s11426-019-9586-3] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 4.7] [Reference Citation Analysis]
41 Krishna Y, Shilpa K, Tanaka F. Intramolecular Mannich and Michael Annulation Reactions of Lactam Derivatives Bearing Enals To Afford Bicyclic N-Heterocycles. Org Lett 2019;21:8444-8. [DOI: 10.1021/acs.orglett.9b03210] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
42 Takahashi Y, Sato T, Chida N. Iridium-catalyzed Reductive Nucleophilic Addition to Tertiary Amides. Chem Lett 2019;48:1138-41. [DOI: 10.1246/cl.190467] [Cited by in Crossref: 24] [Cited by in F6Publishing: 26] [Article Influence: 8.0] [Reference Citation Analysis]
43 Xu Z, Wang XG, Wei YH, Ji KL, Zheng JF, Ye JL, Huang PQ. Organocatalytic, Enantioselective Reductive Bis-functionalization of Secondary Amides: One-Pot Construction of Chiral 2,2-Disubstituted 3-Iminoindoline. Org Lett 2019;21:7587-91. [PMID: 31479277 DOI: 10.1021/acs.orglett.9b02862] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
44 Gabriel P, Gregory AW, Dixon DJ. Iridium-Catalyzed Aza-Spirocyclization of Indole-Tethered Amides: An Interrupted Pictet–Spengler Reaction. Org Lett 2019;21:6658-62. [DOI: 10.1021/acs.orglett.9b02194] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 8.0] [Reference Citation Analysis]
45 Chen TT, Wang AE, Huang PQ. Chemoselective Synthesis of α-Amino-α-cyanophosphonates by Reductive Gem-Cyanation-Phosphonylation of Secondary Amides. Org Lett 2019;21:3808-12. [PMID: 31059269 DOI: 10.1021/acs.orglett.9b01257] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
46 Hou Y, Shi T, Yang Y, Fan X, Chen J, Cao F, Wang Z. Asymmetric Total Syntheses and Biological Studies of Tuberostemoamide and Sessilifoliamide A. Org Lett 2019;21:2952-6. [DOI: 10.1021/acs.orglett.9b01042] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 7.7] [Reference Citation Analysis]
47 Hiraoka S, Matsumoto T, Matsuzaka K, Sato T, Chida N. Approach to Fully Substituted Cyclic Nitrones from N ‐Hydroxylactam Derivatives: Development and Application to the Total Synthesis of Cylindricine C. Angew Chem 2019;131:4425-9. [DOI: 10.1002/ange.201901049] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
48 Yang Z, Lu G, Ye J, Huang P. Ir-catalyzed chemoselective reduction of β-amido esters: A versatile approach to β-enamino esters. Tetrahedron 2019;75:1624-31. [DOI: 10.1016/j.tet.2018.12.024] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
49 Yamamoto S, Komiya Y, Kobayashi A, Minamikawa R, Oishi T, Sato T, Chida N. Asymmetric Total Synthesis of Fasicularin by Chiral N -Alkoxyamide Strategy. Org Lett 2019;21:1868-71. [DOI: 10.1021/acs.orglett.9b00478] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 5.7] [Reference Citation Analysis]
50 Tan K, Yan H, Lu P, Liu Y, Ji R, Liu Z, Li Y, Yu F, Shen Y. Access to Multisubstituted 2(5 H )-Furanones Using Hydrogen Bonding-Promoted Ring-Closing Metathesis and Polyamine Workup. J Org Chem 2019;84:3419-30. [DOI: 10.1021/acs.joc.8b03293] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
51 Hiraoka S, Matsumoto T, Matsuzaka K, Sato T, Chida N. Approach to Fully Substituted Cyclic Nitrones from N-Hydroxylactam Derivatives: Development and Application to the Total Synthesis of Cylindricine C. Angew Chem Int Ed Engl 2019;58:4381-5. [PMID: 30720229 DOI: 10.1002/anie.201901049] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 5.0] [Reference Citation Analysis]
52 Wu H, Yang K, Chen X, Arulkumar M, Wang N, Chen S, Wang Z. A 3,4-dihalo-2(5 H )-furanone initiated ring-opening reaction of DABCO in the absence of a metal catalyst and additive and its application in a one-pot two-step reaction. Green Chem 2019;21:3782-8. [DOI: 10.1039/c9gc01740b] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 4.0] [Reference Citation Analysis]
53 Pelkey ET, Pelkey SJ, Greger JG. Reactions of 3-pyrrolin-2-ones. Advances in Heterocyclic Chemistry 2019. [DOI: 10.1016/bs.aihch.2018.10.004] [Cited by in Crossref: 4] [Article Influence: 1.3] [Reference Citation Analysis]
54 Yang K, Gao J, Luo S, Wu H, Pang C, Wang B, Chen X, Wang Z. Quick construction of a C–N bond from arylsulfonyl hydrazides and C sp2 –X compounds promoted by DMAP at room temperature. RSC Adv 2019;9:19917-23. [DOI: 10.1039/c9ra03403j] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
55 Ma K, Yin X, Dai M. Total Syntheses of Bisdehydroneostemoninine and Bisdehydrostemoninine by Catalytic Carbonylative Spirolactonization. Angew Chem Int Ed Engl 2018;57:15209-12. [PMID: 30230670 DOI: 10.1002/anie.201809114] [Cited by in Crossref: 51] [Cited by in F6Publishing: 53] [Article Influence: 12.8] [Reference Citation Analysis]
56 Ma K, Yin X, Dai M. Total Syntheses of Bisdehydroneostemoninine and Bisdehydrostemoninine by Catalytic Carbonylative Spirolactonization. Angew Chem 2018;130:15429-32. [DOI: 10.1002/ange.201809114] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 3.5] [Reference Citation Analysis]
57 Wu H, Luo S, Cao L, Shi H, Wang B, Wang Z. DABCO‐Mediated C−O Bond Formation from C sp2 ‐Halogen Bond‐Containing Compounds and Alkyl Alcohols. Asian J Org Chem 2018;7:2479-83. [DOI: 10.1002/ajoc.201800517] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
58 Takahashi Y, Yoshii R, Sato T, Chida N. Iridium-Catalyzed Reductive Nucleophilic Addition to Secondary Amides. Org Lett 2018;20:5705-8. [PMID: 30192556 DOI: 10.1021/acs.orglett.8b02421] [Cited by in Crossref: 35] [Cited by in F6Publishing: 38] [Article Influence: 8.8] [Reference Citation Analysis]
59 Trillo P, Slagbrand T, Adolfsson H. Straightforward α-Amino Nitrile Synthesis Through Mo(CO) 6 -Catalyzed Reductive Functionalization of Carboxamides. Angew Chem 2018;130:12527-31. [DOI: 10.1002/ange.201807735] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
60 Trillo P, Slagbrand T, Adolfsson H. Straightforward α-Amino Nitrile Synthesis Through Mo(CO) 6 -Catalyzed Reductive Functionalization of Carboxamides. Angew Chem Int Ed 2018;57:12347-51. [DOI: 10.1002/anie.201807735] [Cited by in Crossref: 37] [Cited by in F6Publishing: 39] [Article Influence: 9.3] [Reference Citation Analysis]
61 Xie LG, Dixon DJ. Iridium-catalyzed reductive Ugi-type reactions of tertiary amides. Nat Commun 2018;9:2841. [PMID: 30026608 DOI: 10.1038/s41467-018-05192-7] [Cited by in Crossref: 54] [Cited by in F6Publishing: 58] [Article Influence: 13.5] [Reference Citation Analysis]
62 Yang ZP, He Q, Ye JL, Huang PQ. Asymmetric Total Synthesis and Absolute Configuration Determination of (-)-Verrupyrroloindoline. Org Lett 2018;20:4200-3. [PMID: 29969900 DOI: 10.1021/acs.orglett.8b01579] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
63 Sato T. How Do You Increase Total Yield in Natural Product Synthesis? J Syn Org Chem , Jpn 2018;76:454-7. [DOI: 10.5059/yukigoseikyokaishi.76.454] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
64 Sugai T, Okuyama Y, Shin J, Usui S, Hisada S, Osanai R, Oishi T, Sato T, Chida N. Synthesis of Kaitocephalin Facilitated by Three Stereoselective Allylic Transposition Reactions. Chem Lett 2018;47:454-7. [DOI: 10.1246/cl.171226] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
65 Oishi T, Yoritate M, Sato T, Chida N. Crystal structure of (-)-(5R,7R,8S,9R,10S)-8-methyl-7-[(5R)-3-methyl-2-oxooxolan-3-en-5-yl]-1-aza-6-oxatri-cyclo-[8.3.0.05,9]tridecan-13-one monohydrate. Acta Crystallogr E Crystallogr Commun 2018;74:555-8. [PMID: 29765766 DOI: 10.1107/S2056989018004425] [Reference Citation Analysis]
66 Wang AE, Yu CC, Chen TT, Liu YP, Huang PQ. Enamines as Surrogates of Alkene Carbanions for the Reductive Alkenylation of Secondary Amides: An Approach to Allylamines. Org Lett 2018;20:999-1002. [PMID: 29384685 DOI: 10.1021/acs.orglett.7b03943] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
67 Meyer AG, Bissember AC, Hyland CJ, Williams CC, Szabo M, Abel SG, Bird MJ, Hyland IK, Pham H. Seven-Membered Rings. Elsevier; 2018. pp. 493-550. [DOI: 10.1016/b978-0-08-102788-2.00016-7] [Cited by in Crossref: 9] [Article Influence: 2.3] [Reference Citation Analysis]
68 Hu X, Shen T, Cai D, Zheng J, Huang P. The iridium-catalysed reductive coupling reaction of tertiary lactams/amides with isocyanoacetates. Org Chem Front 2018;5:2051-6. [DOI: 10.1039/c8qo00312b] [Cited by in Crossref: 26] [Cited by in F6Publishing: 28] [Article Influence: 6.5] [Reference Citation Analysis]
69 Sato T, Yoritate M, Tajima H, Chida N. Total synthesis of complex alkaloids by nucleophilic addition to amides. Org Biomol Chem 2018;16:3864-75. [DOI: 10.1039/c8ob00733k] [Cited by in Crossref: 65] [Cited by in F6Publishing: 68] [Article Influence: 16.3] [Reference Citation Analysis]