Year |
Citation |
Score |
2022 |
Tang J, Ren L, Li J, Wang Y, Hu D, Tong X, Xia C. Photochemical Synthesis of Indolocarbazoles through Tandem Indolization/Dimerization/Mannich Cyclization from Allenes. Organic Letters. PMID 35549288 DOI: 10.1021/acs.orglett.2c01371 |
0.343 |
|
2021 |
Zhang Y, Ye D, Shen L, Liang K, Xia C. Tandem Photoredox-Chiral Phosphoric Acid Catalyzed Radical-Radical Cross-Coupling for Enantioselective Synthesis of 3-Hydroxyoxindoles. Organic Letters. PMID 34459613 DOI: 10.1021/acs.orglett.1c02510 |
0.346 |
|
2021 |
Pan Z, Hu F, Jiang D, Liu Y, Xia C. Chichibabin pyridinium synthesis oxidative decarboxylation of photoexcited α-enamine acids. Chemical Communications (Cambridge, England). PMID 33416811 DOI: 10.1039/d0cc07636h |
0.446 |
|
2020 |
Pan Z, Liu Y, Hu F, Liu Q, Shang W, Ji X, Xia C. Enantioselective Synthesis of Spiroindolines via Cascade Isomerization/Spirocyclization/Dearomatization Reaction. Organic Letters. PMID 31990194 DOI: 10.1021/acs.orglett.0c00181 |
0.376 |
|
2019 |
Tong X, Shi B, Liu Q, Huo Y, Xia C. Retro-biosynthetic construction of corynanthe alkaloid skeletons from rhynchophylline alkaloids. Organic & Biomolecular Chemistry. PMID 31433429 DOI: 10.1039/c9ob01740b |
0.328 |
|
2017 |
Liang K, Xia C. Recent Advances of Transition Metal-Mediated Oxidative Radical Reactions in Total Synthesis of Indole Alkaloids Chinese Journal of Chemistry. 35: 255-270. DOI: 10.1002/CJOC.201600777 |
0.31 |
|
2016 |
Liang K, Wu T, Xia C. Concise total synthesis of (±)-serotobenine. Organic & Biomolecular Chemistry. PMID 27121362 DOI: 10.1039/c6ob00682e |
0.312 |
|
2016 |
Liang K, Yang J, Tong X, Shang W, Pan Z, Xia C. Biomimetic Synthesis of Moschamine-Related Indole Alkaloids via Iron-Catalyzed Selectively Oxidative Radical Coupling. Organic Letters. PMID 26949004 DOI: 10.1021/acs.orglett.6b00417 |
0.336 |
|
2014 |
Deng X, Liang K, Tong X, Ding M, Li D, Xia C. Copper-catalyzed radical cyclization to access 3-hydroxypyrroloindoline: biomimetic synthesis of protubonine A. Organic Letters. 16: 3276-9. PMID 24922604 DOI: 10.1021/ol501287x |
0.344 |
|
2013 |
Tong X, Ni G, Deng X, Xia C. ChemInform Abstract: Access to Ynamides via CuO-Mediated Oxidative Amidation of Alkynes. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201305051 |
0.311 |
|
2010 |
Ma D, Xia C, Jiang J, Zhang J. ChemInform Abstract: First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200142235 |
0.516 |
|
2010 |
Ma D, Xia C, Tian H. ChemInform Abstract: Oxidation of Benzylic Methylene Compounds to Ketones with m-Chloroperoxybenzoic Acid and Oxygen. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200009060 |
0.613 |
|
2003 |
Ma D, Xia C, Jiang J, Zhang J, Tang W. Aromatic nucleophilic substitution or CuI-catalyzed coupling route to martinellic acid. The Journal of Organic Chemistry. 68: 442-51. PMID 12530870 DOI: 10.1021/Jo026125Z |
0.626 |
|
2003 |
Xia C, Heng L, Ma D. Total Synthesis of (.+-.)-Martinelline. Cheminform. 34. DOI: 10.1002/CHIN.200312187 |
0.462 |
|
2002 |
Xia C, Heng L, Ma D. Total synthesis of (±)-martinelline Tetrahedron Letters. 43: 9405-9409. DOI: 10.1016/S0040-4039(02)02331-6 |
0.56 |
|
2001 |
Ma D, Xia C. CuI-catalyzed coupling reaction of β-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857 Organic Letters. 3: 2583-2586. PMID 11483066 DOI: 10.1021/Ol016258R |
0.593 |
|
2001 |
Ma D, Xia C, Jiang J, Zhang J. First total synthesis of martinellic acid, a naturally occurring bradykinin receptor antagonist. Organic Letters. 3: 2189-91. PMID 11440576 DOI: 10.1021/Ol016043H |
0.615 |
|
1999 |
Xu J, Xia C, Yu L, Zhou Q. SYNTHESIS OF PHOSPHONOPEPTIDES CONTAINING 1-AMINOALKYLPHOSPHONIC ACID Phosphorus, Sulfur, and Silicon and the Related Elements. 152: 35-44. DOI: 10.1080/10426509908031615 |
0.412 |
|
1999 |
Ma D, Xia C, Tian H. Oxidation of benzylic methylene compounds to ketones with m-chloroperoxybenzoic acid and oxygen Tetrahedron Letters. 40: 8915-8917. DOI: 10.1016/S0040-4039(99)01886-9 |
0.625 |
|
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