Research graph
References from Base and Nucleophilic Catalysis Enables Formal [3+2] Cycloaddition of Alkynyl Diazoketones and Aminomalonates: Access to γ,γ‐Disubstituted 3‐Pyrrolin‐2‐ones. Local targets link to admitted publications; unresolved targets remain external evidence.
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10.1021/acschembio.6b00596 · External reference
Exploring the Synthetic Potential of γ‐Lactam Derivatives Obtained From a Multicomponent Reaction‐Applications as Antiproliferative Agents
10.3390/molecules27113624 · 2022 · External reference
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Lactacystin, a Novel Microbial Metabolite, Induces Neuritogenesis of Neuroblastoma Cells
10.7164/antibiotics.44.113 · 1991 · External reference
Structure of Lactacystin, a New Microbial Metabolite Which Induces Differentiation of Neuroblastoma Cells
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10.1039/c7cc01058c · External reference
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10.1002/ajoc.202100187 · External reference
10.1021/acs.orglett.2c01898
10.1021/acs.orglett.2c01898 · External reference
10.3390/molecules28073162
10.3390/molecules28073162 · External reference
10.1039/d3qo01909h
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10.1039/d5ob01300c · External reference
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10.1021/acs.orglett.5c03109 · External reference
10.1002/adsc.202401183
10.1002/adsc.202401183 · External reference
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10.1039/d0cs00224k · External reference
10.1021/acs.chemrev.7b00382
10.1021/acs.chemrev.7b00382 · External reference
10.1002/ajoc.201800472
10.1002/ajoc.201800472 · External reference
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10.1039/c5cs00821b · External reference
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10.1002/cjoc.202300716 · External reference
10.1021/acscatal.1c04746
10.1021/acscatal.1c04746 · External reference
Catalytic Reactions for Enantioselective Transfers of Donor‐Substituted Carbenes
10.1016/j.checat.2022.10.016 · 2022 · External reference
Silver Carbenoids Derived From Diazo Compounds: A Historical Perspective on Challenges and Opportunities
10.1016/j.checat.2021.05.001 · 2021 · External reference
10.1021/acs.accounts.2c00186
10.1021/acs.accounts.2c00186 · External reference
10.1016/j.tetlet.2022.154135
10.1016/j.tetlet.2022.154135 · External reference
10.13822/j.cnki.hxsj.2025.0187
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10.1021/ol802614j · External reference
10.1038/s41467‐021‐27167‐x
10.1038/s41467‐021‐27167‐x · External reference
10.1021/acs.orglett.2c00477
10.1021/acs.orglett.2c00477 · External reference
10.1039/d5cc00594a
10.1039/d5cc00594a · External reference
10.1002/jlac.19123940104
10.1002/jlac.19123940104 · External reference
10.1002/poc.1875
10.1002/poc.1875 · External reference
10.1002/1099‐0690(200207)2002:14<2193::aid‐ejoc2193>3.0.co;2‐d
10.1002/1099‐0690(200207)2002:14<2193::aid‐ejoc2193>3.0.co;2‐d · External reference
10.1021/jacs.7b08310
10.1021/jacs.7b08310 · External reference
10.1002/cjoc.70328
10.1002/cjoc.70328 · External reference
10.1002/anie.202400805
10.1002/anie.202400805 · External reference
10.1021/acs.orglett.6c00595
10.1021/acs.orglett.6c00595 · External reference
10.1002/cjoc.70755 · Admitted local publication
10.1021/jacs.6c11390
10.1021/jacs.6c11390 · External reference
10.1021/acs.orglett.5c03721
10.1021/acs.orglett.5c03721 · External reference
10.1021/acs.orglett.6c00343
10.1021/acs.orglett.6c00343 · External reference
10.1039/d6cc05248g
10.1039/d6cc05248g · External reference
10.1021/ja984021t
10.1021/ja984021t · External reference
10.1021/ja012427r
10.1021/ja012427r · External reference
10.1021/ja027466x
10.1021/ja027466x · External reference
