| Year |
Citation |
Score |
| 2023 |
Sit MK, Cao HH, Wu YD, Yip TC, Bendel LE, Zhang W, Dai WM. Synthesis of the Macrolactone Cores of Maltepolides via a Diene-Ene Ring-Closing Metathesis Strategy. Organic Letters. PMID 36820513 DOI: 10.1021/acs.orglett.3c00106 |
0.556 |
|
| 2019 |
Xu J, Lin B, Jiang X, Jia Z, Wu J, Dai WM. Intramolecular Diels-Alder Cycloaddition Approach toward the cis-Fused Δ-Hexahydroisoindol-1-one Core of Cytochalasins. Organic Letters. PMID 30645139 DOI: 10.1021/Acs.Orglett.8B04129 |
0.408 |
|
| 2018 |
Su Y, Dai W. Synthesis of the C18–C26 tetrahydrofuran-containing fragment of amphidinolide C congeners via tandem asymmetric dihydroxylation and SN2 cyclization Tetrahedron. 74: 1546-1554. DOI: 10.1016/J.Tet.2018.02.021 |
0.48 |
|
| 2016 |
Jiang X, Dai W, Zhao J, Shi F. Brønsted acid catalyzed reaction of ortho-hydroxylstyrenes with indoles: Synthesis of 1,1-diarylethanes Chinese Journal of Organic Chemistry. 36: 1014-1020. DOI: 10.6023/cjoc201601002 |
0.325 |
|
| 2014 |
Han W, Wu J, Dai W. Synthesis of Highly Functionalized Benzofuran-2-carboxamides by Ugi Four-Component Reaction and Microwave-Assisted Rap–Stoermer Reaction Synlett. 25: 2019-2024. DOI: 10.1055/S-0034-1378351 |
0.475 |
|
| 2014 |
Xu J, Li X, Wu J, Dai W. Synthesis of 5-alkyl-5-aryl-1-pyrroline N-oxides from 1-aryl-substituted nitroalkanes and acrolein via Michael addition and nitro reductive cyclization Tetrahedron. 70: 6384-6391. DOI: 10.1016/J.Tet.2014.07.046 |
0.443 |
|
| 2014 |
Xu J, Li X, Wu J, Dai W. Synthesis of 5-alkyl-5-aryl-γ-lactams from 1-aryl-substituted nitroalkanes and methyl acrylate via Michael addition and reductive lactamization Tetrahedron. 70: 3839-3846. DOI: 10.1016/J.Tet.2014.04.074 |
0.433 |
|
| 2014 |
Wang Y, Dai W. Synthesis of the Conjugated Tetraene Acid Side Chain of Mycolactone E by Suzuki–Miyaura Cross-Coupling Reaction of Alkenyl Boronates (Eur. J. Org. Chem. 2/2014) European Journal of Organic Chemistry. 2014. DOI: 10.1002/Ejoc.201490000 |
0.386 |
|
| 2014 |
Wang Y, Dai W. Synthesis of the Conjugated Tetraene Acid Side Chain of Mycolactone E by Suzuki–Miyaura Cross‐Coupling Reaction of Alkenyl Boronates European Journal of Organic Chemistry. 2014: 323-330. DOI: 10.1002/Ejoc.201301484 |
0.448 |
|
| 2013 |
Yu G, Zheng Y, Wu J, Dai W. Increasing appendage diversity on 3,4-dihydro-3-oxo-2H-1,4-benzoxazines via Aphos–Pd(OAc)2-catalyzed Suzuki–Miyaura cross-coupling of aryl chlorides Tetrahedron. 69: 10488-10496. DOI: 10.1016/J.Tet.2013.09.057 |
0.44 |
|
| 2013 |
Ye N, Dai W. An Efficient and Reliable Catalyst System Using Hemilabile Aphos for B‐Alkyl Suzuki–Miyaura Cross‐Coupling Reaction with Alkenyl Halides (Eur. J. Org. Chem. 5/2013) European Journal of Organic Chemistry. 2013. DOI: 10.1002/Ejoc.201390009 |
0.342 |
|
| 2013 |
Ye N, Dai WM. An Efficient and Reliable Catalyst System Using Hemilabile Aphos for B-Alkyl Suzuki-Miyaura Cross-Coupling Reaction with Alkenyl Halides European Journal of Organic Chemistry. 831-835. DOI: 10.1002/Ejoc.201201602 |
0.45 |
|
| 2013 |
Wu D, Wu J, Dai W. Cover Picture: A Concise Total Synthesis of Amphidinin B (Chin. J. Chem. 1/2013) Chinese Journal of Chemistry. 31: 1-1. DOI: 10.1002/Cjoc.201390000 |
0.31 |
|
| 2013 |
Wu D, Wu J, Dai W. A Concise Total Synthesis of Amphidinin B Chinese Journal of Chemistry. 31: 105-110. DOI: 10.1002/Cjoc.201201069 |
0.343 |
|
| 2012 |
Zhao G, Wu J, Dai W. Toward a Total Synthesis of Divergolide A; Synthesis of the Amido Hydro-quinone Core and the C10–C15 Fragment Synlett. 23: 2845-2849. DOI: 10.1055/S-0032-1317491 |
0.477 |
|
| 2011 |
Dai J, Wu J, Zhao G, Dai WM. In(OTf)3-catalyzed highly chemo- and regioselective head-to-tail heterodimerization of vinylarenes with 1,1-diarylethenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 8290-3. PMID 21656598 DOI: 10.1002/Chem.201101190 |
0.338 |
|
| 2011 |
Liu Y, Feng G, Wang J, Wu J, Dai W. Synthesis of Two Diastereomers of Iriomoteolide-1a via a Tunable Four-Module Coupling Approach Using Ring-Closing Metathesis as the Key Step Synlett. 2011: 1774-1778. DOI: 10.1055/S-0030-1260822 |
0.615 |
|
| 2011 |
Wu D, Li H, Jin J, Wu J, Dai W. Total Synthesis of AmphidinolideT3 Using Ring-Closing Metathesis and Asymmetric DihydroxylationStrategy Synlett. 2011: 895-898. DOI: 10.1055/S-0030-1259706 |
0.4 |
|
| 2011 |
Wu J, Jiang X, Xu J, Dai W. Tandem Wittig–intramolecular Diels–Alder cycloaddition of ester-tethered 1,3,9-decatrienes under microwave heating Tetrahedron. 67: 179-192. DOI: 10.1016/J.Tet.2010.10.088 |
0.397 |
|
| 2010 |
Li H, Wu J, Luo J, Dai WM. A concise total synthesis of amphidinolide T2. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 11530-4. PMID 20803588 DOI: 10.1002/Chem.201001794 |
0.381 |
|
| 2010 |
Liu Y, Wang J, Li H, Wu J, Feng G, Dai W. Synthesis of the C7-C23Fragment Related to Iriomoteolide-1a via B-Alkyl Suzuki-MiyauraCross-Coupling and Indium-Mediated Aldehyde Allylation Synlett. 2010: 2184-2188. DOI: 10.1055/S-0030-1258507 |
0.551 |
|
| 2010 |
Zheng Y, Yu G, Wu J, Dai W. Synthesis of N-Arylisoindolin-1-onesvia Pd-Catalyzed Intramolecular Decarbonylative Couplingof N-(2-Bromobenzyl)oxanilic Acid PhenylEsters Synlett. 2010: 1075-1080. DOI: 10.1055/S-0029-1219580 |
0.375 |
|
| 2010 |
Wang Y, Dai W. Total synthesis of diastereomeric marine butenolides possessing a syn-aldol subunit at C10 and C11 and the related C11-ketone Tetrahedron. 66: 187-196. DOI: 10.1016/J.Tet.2009.10.115 |
0.467 |
|
| 2010 |
Dai W, Mak W. Structural Effect on Eu(fod)3‐Catalyzed Rearrangement of Allylic Esters Chinese Journal of Chemistry. 21: 772-783. DOI: 10.1002/Cjoc.20030210713 |
0.354 |
|
| 2009 |
Wang Y, Wu J, Dai W. Stereoselectivity of Intramolecular Diels-Alder Reaction of Hydroxamate-Tethered 1,3,9-Decatrienes under Thermal and Microwave Heating Synlett. 2009: 2862-2866. DOI: 10.1055/S-0029-1217966 |
0.442 |
|
| 2009 |
Sun L, Feng G, Guan Y, Liu Y, Wu J, Dai W. Influence of Appended Groups on the Formation of 16-Membered Macrolactone Core Related to the Plecomacrolides via Diene-Ene Ring-Closing Metathesis Synlett. 2009: 2361-2365. DOI: 10.1055/S-0029-1217720 |
0.546 |
|
| 2009 |
Dai W, Wu J, Jiang Y. Assembly of 1,3-Dihydro-2H-3-benzazepin-2-one Conjugates via Ugi Four-Component Reaction and Palladium-Catalyzed Hydroamidation¹ Synlett. 2009: 1162-1166. DOI: 10.1055/S-0028-1088115 |
0.456 |
|
| 2009 |
Sun L, Wu J, Dai W. Synthesis of C18–C28 ketone fragment of micromonospolide B possessing 1,3-diene and 1,3-anti-diol functionalities Tetrahedron-Asymmetry. 20: 1864-1870. DOI: 10.1016/J.Tetasy.2009.07.042 |
0.431 |
|
| 2009 |
Luo J, Li H, Wu J, Xing X, Dai W. Synthesis of the C1–C12 acid fragment of amphidinolide T marine macrolides via SmI2-mediated enantioselective reductive coupling of aldehydes with a chiral crotonate Tetrahedron. 65: 6828-6833. DOI: 10.1016/J.Tet.2009.06.070 |
0.441 |
|
| 2008 |
Dai WM, Li Y, Zhang Y, Yue C, Wu J. Generation of an aromatic amide-derived phosphane (Aphos) library by self-assisted molecular editing and applications of Aphos in room-temperature Suzuki-Miyaura reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 5538-54. PMID 18478517 DOI: 10.1002/Chem.200800318 |
0.6 |
|
| 2008 |
Dai W, Chen Y, Jin J, Wu J, Lou J, He Q. Total Synthesis of Amphidinolide X and Its 12Z-Isomer by Formation of the C12-C13 Trisubstituted Double Bond via Ring-Closing Metathesis Synlett. 2008: 1737-1741. DOI: 10.1055/S-2008-1077885 |
0.409 |
|
| 2008 |
Dai W, Feng G, Wu J, Sun L. Synthesis of C3-C12 Fragment of 24-Demethylbafilomycin C1 via anti-Selective Aldol Condensation as the Key Stereocontrol Step Synlett. 2008: 1013-1016. DOI: 10.1055/S-2008-1072504 |
0.581 |
|
| 2008 |
Dai W, Shi J, Wu J. Synthesis of 3-Arylideneindolin-2-onesfrom 2-Aminophenols by Ugi Four-Component Reaction andHeck Carbocyclization Synlett. 2008: 2716-2720. DOI: 10.1055/S-0028-1083505 |
0.453 |
|
| 2008 |
Dai W, Shi L, Li Y. Total synthesis of (4S,10R)-4-hydroxy-10-methyl-11-oxododec-2-en-1,4-olide and related bioactive marine butenolides Tetrahedron-Asymmetry. 19: 1549-1556. DOI: 10.1016/J.Tetasy.2008.06.028 |
0.415 |
|
| 2007 |
Dai WM, Shi J. Diversity-oriented synthesis and solid-phase organic synthesis under controlled microwave heating. Combinatorial Chemistry & High Throughput Screening. 10: 837-56. PMID 18288947 DOI: 10.2174/138620707783220338 |
0.427 |
|
| 2007 |
Jin J, Chen Y, Li Y, Wu J, Dai WM. Total synthesis of amphidinolide Y by formation of trisubstituted (E)-double bond via ring-closing metathesis of densely functionalized alkenes. Organic Letters. 9: 2585-8. PMID 17536814 DOI: 10.1021/Ol0710360 |
0.437 |
|
| 2007 |
Guan Y, Wu J, Sun L, Dai WM. Synthesis of C13-C25 fragment of 24-demethylbafilomycin C(1) via diastereoselective aldol reactions of a ketone boron enolate as the key step. The Journal of Organic Chemistry. 72: 4953-60. PMID 17518500 DOI: 10.1021/Jo070624O |
0.565 |
|
| 2007 |
Wu J, Nie L, Luo J, Dai W. Microwave-assisted, palladium-catalyzed intramolecular direct arylation for the synthesis of novel fused heterocycles Synlett. 2007: 2728-2732. DOI: 10.1055/S-2007-991053 |
0.492 |
|
| 2007 |
Wu J, Yu H, Wang Y, Xing X, Dai W. Unexpected epimerization and stereochemistry revision of IMDA adducts from sorbate-related 1,3,8-nonatrienes Tetrahedron Letters. 48: 6543-6547. DOI: 10.1016/J.Tetlet.2007.07.046 |
0.407 |
|
| 2007 |
Feng G, Wu J, Dai W. Isolation and characterization of 2-alkylaminobenzo[b]furans. Evidence for competing O-arylation in Cu-catalyzed intramolecular amidation Tetrahedron Letters. 48: 401-404. DOI: 10.1016/J.Tetlet.2006.11.084 |
0.524 |
|
| 2007 |
Dai W, Li H. Lewis acid-catalyzed formation of Ugi four-component reaction product from Passerini three-component reaction system without an added amine Tetrahedron. 63: 12866-12876. DOI: 10.1016/J.Tet.2007.10.050 |
0.354 |
|
| 2006 |
Sun LP, Dai WM. An engineered linker capable of promoting on-resin reactions for microwave-assisted solid-phase organic synthesis. Angewandte Chemie (International Ed. in English). 45: 7255-8. PMID 17024715 DOI: 10.1002/Anie.200602523 |
0.513 |
|
| 2006 |
Zhang Y, Wang Y, Dai WM. Efficient remote axial-to-central chirality transfer in enantioselective SmI2-mediated reductive coupling of aldehydes with crotonates of atropisomeric 1-naphthamides. The Journal of Organic Chemistry. 71: 2445-55. PMID 16526796 DOI: 10.1021/Jo0526486 |
0.444 |
|
| 2006 |
Tachi Y, Dai WM, Tanabe K, Nishimoto S. Synthesis and DNA cleavage reaction characteristics of enediyne prodrugs activated via an allylic rearrangement by base or UV irradiation. Bioorganic & Medicinal Chemistry. 14: 3199-209. PMID 16413193 DOI: 10.1016/J.Bmc.2005.12.040 |
0.38 |
|
| 2006 |
Xing X, Wu J, Luo J, Dai W. C-N bond-linked conjugates of dibenz[b,f][1,4]oxazepines with 2-oxindole Synlett. 2006: 2099-2103. DOI: 10.1055/S-2006-948172 |
0.338 |
|
| 2006 |
Chen Y, Jin J, Wu J, Dai W. A New Synthesis of Tetrahydrofuran Fragment of Amphidinolides X and Y Synlett. 2006: 1177-1180. DOI: 10.1055/S-2006-932487 |
0.408 |
|
| 2006 |
Xing X, Wu J, Dai W. Acid-mediated three-component aza-Diels–Alder reactions of 2-aminophenols under controlled microwave heating for synthesis of highly functionalized tetrahydroquinolines. Part 9: Chemistry of aminophenols Tetrahedron. 62: 11200-11206. DOI: 10.1016/J.Tet.2006.09.012 |
0.454 |
|
| 2006 |
Wu J, Sun L, Dai W. Microwave-assisted tandem Wittig–intramolecular Diels–Alder cycloaddition. Product distribution and stereochemical assignment Tetrahedron. 62: 8360-8372. DOI: 10.1016/J.Tet.2006.06.039 |
0.578 |
|
| 2006 |
Xing X, Wu J, Feng G, Dai W. Microwave-assisted one-pot U-4CR and intramolecular O-alkylation toward heterocyclic scaffolds Tetrahedron. 62: 6774-6781. DOI: 10.1016/J.Tet.2006.05.001 |
0.566 |
|
| 2006 |
Wu J, Li D, Wu H, Sun L, Dai W. Microwave-assisted regioselective olefinations of cyclic mono- and di-ketones with a stabilized phosphorus ylide Tetrahedron. 62: 4643-4650. DOI: 10.1016/J.Tet.2005.12.060 |
0.698 |
|
| 2006 |
Feng G, Wu J, Dai W. One-pot regioselective annulation toward 3,4-dihydro-3-oxo-2H-1,4-benzoxazine scaffolds under controlled microwave heating Tetrahedron. 62: 4635-4642. DOI: 10.1016/J.Tet.2005.12.059 |
0.588 |
|
| 2005 |
Dai WM, Guan Y, Jin J. Structures and total syntheses of the plecomacrolides. Current Medicinal Chemistry. 12: 1947-93. PMID 16101499 DOI: 10.2174/0929867054546591 |
0.35 |
|
| 2005 |
Dai W, Zhang Y. A family of simple amide-derived air-stable P,O-ligands for Suzuki cross-coupling of unactivated aryl chlorides Tetrahedron Letters. 46: 1377-1381. DOI: 10.1016/J.Tetlet.2004.12.133 |
0.426 |
|
| 2005 |
Dai W, Wang X, Ma C. Microwave-assisted one-pot regioselective synthesis of 2-alkyl-3,4-dihydro-3-oxo-2H-1,4-benzoxazines Tetrahedron. 61: 6879-6885. DOI: 10.1016/J.Tet.2005.04.072 |
0.466 |
|
| 2004 |
Dai W, Tachi Y, Nishimoto S, Zhong X, Guo Z. Synthesis and Cytotoxicity of Enediyne Prodrugs with 3-Hydroxy-4-(arylmethylidene)cyclodeca-1,5-diyne Scaffolds Letters in Drug Design & Discovery. 1: 69-72. DOI: 10.2174/1570180043485699 |
0.378 |
|
| 2004 |
Wu J, Wu H, Wei S, Dai W. Highly regioselective Wittig reactions of cyclic ketones with a stabilized phosphorus ylide under controlled microwave heating Tetrahedron Letters. 45: 4401-4404. DOI: 10.1016/J.Tetlet.2004.03.198 |
0.613 |
|
| 2004 |
Dai WM, Li Y, Zhang Y, Lai KW, Wu J. A novel class of amide-derived air-stable P,O-ligands for Suzuki cross-coupling at low catalyst loading Tetrahedron Letters. 45: 1999-2001. DOI: 10.1016/J.Tetlet.2003.12.142 |
0.371 |
|
| 2004 |
Dai W, Yeung KKY, Wang Y. The first example of atropisomeric amide-derived P,O-ligands used for an asymmetric Heck reaction Tetrahedron. 60: 4425-4430. DOI: 10.1016/J.Tet.2004.02.062 |
0.422 |
|
| 2004 |
Haruna K, Tanabe K, Ishii A, Dai W, Hatta H, Nishimoto S. Corrigendum to “Photo-induced DNA cleavage reaction characteristics of propargylic sulfones possessing anthraquinone chromophore”: [Bioorg. Med. Chem. 11 (2003) 5311–5316] Bioorganic & Medicinal Chemistry. 12: 2489. DOI: 10.1016/J.Bmc.2004.03.001 |
0.335 |
|
| 2003 |
Dai WM. Natural product inspired design of enediyne prodrugs via rearrangement of an allylic double bond. Current Medicinal Chemistry. 10: 2265-83. PMID 14529342 DOI: 10.2174/0929867033456756 |
0.376 |
|
| 2003 |
Dai WM, Guo DS, Sun LP, Huang XH. Microwave-assisted solid-phase organic synthesis (MASPOS) as a key step for an indole library construction. Organic Letters. 5: 2919-22. PMID 12889908 DOI: 10.1021/Ol0350543 |
0.561 |
|
| 2003 |
Dai WM, Yeung KKY, Leung WH, Haynes RK. Air-stable P-stereogenic secondary phosphine oxides as chiral monodentate ligands for asymmetric catalytic carbon-carbon bond formation Tetrahedron Asymmetry. 14: 2821-2826. DOI: 10.1016/J.Tetasy.2003.07.008 |
0.31 |
|
| 2002 |
Dai WM, Yeung KK, Liu JT, Zhang Y, Williams ID. A novel class of nonbiaryl atropisomeric P,O-ligands for palladium-catalyzed asymmetric allylic alkylation. Organic Letters. 4: 1615-8. PMID 11975642 DOI: 10.1021/Ol0258233 |
0.368 |
|
| 2002 |
Dai W, Wu A, Wu H. Asymmetric Wittig reactions of chiral arsonium ylides. Part 3: Reversal of stereochemistry caused by metal cation in enantioselective olefination of 4-substituted cyclohexanones using a C2-symmetric chiral arsine ☆ Tetrahedron-Asymmetry. 13: 2187-2191. DOI: 10.1016/S0957-4166(02)00588-8 |
0.468 |
|
| 2002 |
Dai WM, Lai KW. Chemistry of aminophenols. Part 3: First synthesis of nitrobenzo[b]furans via a coupling-cyclization approach Tetrahedron Letters. 43: 9377-9380. DOI: 10.1016/S0040-4039(02)02333-X |
0.407 |
|
| 2002 |
Dai W, Sun L, Guo D. Chemistry of aminophenols. Part 2: A general and efficient synthesis of indoles possessing a nitrogen substituent at the C4, C5, C6, and C7 positions Tetrahedron Letters. 43: 7699-7702. DOI: 10.1016/S0040-4039(02)01851-8 |
0.415 |
|
| 2001 |
Dai W, Yeung KKY, Chow CW, Williams ID. Study on enantiomerically pure 2-substituted N,N-dialkyl-1-naphthamides: resolution, absolute stereochemistry, and application to desymmetrization of cyclic meso anhydrides Tetrahedron: Asymmetry. 12: 1603-1613. DOI: 10.1016/S0957-4166(01)00278-6 |
0.363 |
|
| 2001 |
Dai W, Guo D, Sun L. Chemistry of aminophenols. Part 1: Remarkable additive effect on Sonogashira cross-coupling of 2-carboxamidoaryl triflates and application to novel synthesis of indoles Tetrahedron Letters. 42: 5275-5278. DOI: 10.1016/S0040-4039(01)00965-0 |
0.462 |
|
| 2001 |
Dai WM, Wu A, Lee MYH, Lai KW. Neighboring nucleophilic group assisted rearrangement of allylic esters under Eu(fod)3 catalysis Tetrahedron Letters. 42: 4215-4218. DOI: 10.1016/S0040-4039(01)00708-0 |
0.376 |
|
| 2001 |
Dai W, Wu A, Hamaguchi W. Intramolecular Nozaki–Hiyama–Kishi reactions and Ln(III)-catalyzed allylic rearrangement as the key steps towards 10-membered ring enediynes Tetrahedron Letters. 42: 4211-4214. DOI: 10.1016/S0040-4039(01)00707-9 |
0.485 |
|
| 2000 |
Dai W, Zhu H, Hao X. Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral β-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes Tetrahedron-Asymmetry. 11: 2315-2337. DOI: 10.1016/S0957-4166(00)00189-0 |
0.369 |
|
| 1999 |
Dai WM, Fong KC, Lau CW, Zhou L, Hamaguchi W, Nishimoto Si. Synthesis and DNA Cleavage Study of a 10-Membered Ring Enediyne Formed via Allylic Rearrangement. The Journal of Organic Chemistry. 64: 682-683. PMID 11674126 DOI: 10.1021/Jo9820263 |
0.384 |
|
| 1999 |
Zhou L, Ino A, Dai WM, Nishimoto S. Evidences for adduct formation between intracellular non-protein thiols and nitroazoles possessing an alpha,beta-unsaturated carbonyl side chain and the effects on radiosensitization of hypoxic cells. Bioorganic & Medicinal Chemistry. 7: 2591-8. PMID 10632069 DOI: 10.1016/S0968-0896(99)00187-X |
0.316 |
|
| 1999 |
Dai WM, Chow CW, Zhou L, Ishii A, Lau CW, Li Q, Hamaguchi W, Nishimoto S. Bifunctional 2-naphthyl propargylic sulfones exhibiting high DNA intercalating and alkylating activity. Bioorganic & Medicinal Chemistry Letters. 9: 2789-94. PMID 10522692 DOI: 10.1016/S0960-894X(99)00475-8 |
0.315 |
|
| 1999 |
Dai WM, Wu J, Fong KC, Lee MYH, Lau CW. Regioselective synthesis of acyclic cis-enediynes via an acid-catalyzed rearrangement of 1,2-dialkynylallyl alcohols. Syntheses, computational calculations, and mechanism Journal of Organic Chemistry. 64: 5062-5082. DOI: 10.1021/Jo982476V |
0.388 |
|
| 1999 |
Dai W, Lee MYH. Eu(fod)3-Catalyzed rearrangement of allylic esters possessing a chelating site. Application to enediyne synthesis Tetrahedron Letters. 40: 2397-2400. DOI: 10.1016/S0040-4039(99)00276-2 |
0.479 |
|
| 1998 |
Dai WM, Li Q, Fong KC, Chow CW, Zhou L, Hamaguchi W, Nishimoto S. Remarkable tethering effect on DNA cleavage of propargylic sulfone conjugates with intercalating moieties. Bioorganic & Medicinal Chemistry Letters. 8: 169-74. PMID 9871648 DOI: 10.1016/S0960-894X(97)10203-7 |
0.321 |
|
| 1998 |
Zhu H, Zhao B, Dai W, Zhou J, Hao X. Chiral ligands derived from abrine. Part 5: Substituent effects on asymmetric induction in enantioselective addition of diethylzinc to benzaldehyde catalyzed by chiral oxazolidines possessing an indole moiety Tetrahedron-Asymmetry. 9: 2879-2888. DOI: 10.1016/S0957-4166(98)00298-5 |
0.432 |
|
| 1998 |
Dai W, Lee MYH. Regiocontrolled synthesis of cis-enediynes via intramolecular trapping of allylic cations Tetrahedron Letters. 39: 8149-8152. DOI: 10.1016/S0040-4039(98)01834-6 |
0.379 |
|
| 1998 |
Dai W, Wu J, Wu A. Two distinct epoxide ring opening pathways in a monocyclic model system of the kedarcidin chromophore Tetrahedron Letters. 39: 4091-4094. DOI: 10.1016/S0040-4039(98)00664-9 |
0.35 |
|
| 1996 |
Dai W, Zhu HJ, Hao X. Chiral ligands derived from Abrine .2. Oxazolidines as promoters for enantioselective addition of diethylzinc toward aromatic aldehydes Tetrahedron-Asymmetry. 7: 1245-1248. DOI: 10.1016/0957-4166(96)00133-4 |
0.414 |
|
| 1996 |
Dai W, Fong KC. First synthesis of cis-enediynes from 1,5-diynes by an acid-mediated allylic rearrangement Tetrahedron Letters. 37: 8413-8416. DOI: 10.1016/0040-4039(96)01924-7 |
0.403 |
|
| 1996 |
Dai W, Zhu HJ, Hao X. Chiral ligands derived from Abrine .3. Asymmetric Pictet-Spengler reaction of Abrine methyl ester and synthesis of chiral 1,2,3,4-tetrahydro-beta-carbolines as promoters in addition of diethylzinc toward aromatic aldehydes Tetrahedron Letters. 37: 5971-5974. DOI: 10.1016/0040-4039(96)01290-7 |
0.445 |
|
| 1996 |
Dai W, Fong KC, Danjo H, Nishimoto S. Synthesis of cis‐Enediynes from 1,5‐Diynes by Rearrangement of an Allylic Double Bond Angewandte Chemie. 35: 779-781. DOI: 10.1002/Anie.199607791 |
0.37 |
|
| 1996 |
Dai W, Fong KC, Danjo H, Nishimoto S. Synthese von cis‐Endiinen durch Umlagerung einer allylischen Doppelbindung Angewandte Chemie. 108: 821-822. DOI: 10.1002/Ange.19961080717 |
0.333 |
|
| 1995 |
Dai W, Lau CW, Chung SH, Wu YD. Influence of Alkyl Substituent on the Asynchronous Transition Structure of Boron-Catalyzed Diels-Alder Cycloaddition of .alpha.,.beta.-Unsaturated Aldehydes with 1,1-Dimethyl-1,3-butadiene Derivatives Journal of Organic Chemistry. 60: 8128-8129. DOI: 10.1021/Jo00130A006 |
0.321 |
|
| 1995 |
Dai W, Zhu HJ, Hao X. Chiral ligands derived from Abrine. 1. Synthesis of sec- and tert-β-amino alcohols and catalysis for enantioselective addition of diethylzinc toward aromatic aldehydes Tetrahedron-Asymmetry. 6: 1857-1860. DOI: 10.1016/0957-4166(95)00236-I |
0.373 |
|
| 1995 |
Dai W, Fong KC. Synthesis, Reaction, And Cytotoxicity Of Novel Propargylic Sulfones Tetrahedron Letters. 36: 5613-5616. DOI: 10.1016/0040-4039(95)01169-I |
0.397 |
|
| 1995 |
Dai W, Cheung YK, Tang KW, Choi PY, Chung SL. Highly Chemoselective Acylation of Substituted Aminophenols with 3-(Trimethylacetyl)-1,3-thiazolidine-2-thione Tetrahedron. 51: 12263-12276. DOI: 10.1016/0040-4020(95)00783-5 |
0.395 |
|
| 1992 |
Nicolaou KC, Maligres P, Suzuki T, Wendeborn SV, Dai WM, Chadha RK. Molecular design and chemical synthesis of potent enediynes. 1. Dynemicin model systems equipped with N-tethered triggering devices Journal of the American Chemical Society. 114: 8890-8907. DOI: 10.1021/Ja00049A022 |
0.376 |
|
| 1990 |
Nagao Y, Dai W, Ochiai M, Shiro M. Diastereoselective alkylation of chiral tin (II) enolates onto cyclic acyl iminium ions. Asymmetric total synthesis of (-)-supinidine Tetrahedron. 46: 6361-6380. DOI: 10.1016/S0040-4020(01)96008-9 |
0.4 |
|
| 1985 |
Dai W, Zhou W. New synthesis of two optically active steroid CD ring synthons by microbial asymmetric reduction Tetrahedron. 41: 4475-4482. DOI: 10.1016/S0040-4020(01)82341-3 |
0.369 |
|
| Show low-probability matches. |