分子合成化学研究室

Keyphrases

1. 1,2-cis 9%
2. 1,3-Cyclohexanedione 20%
3. 1,3-Diones 8%
4. 1,3-dipolar Cycloaddition 16%
5. 2,3-Sigmatropic Rearrangement 11%
6. 2-Iodobenzamides 19%
7. 2-substituted 9%
8. Acetal 16%
9. Alcohol 10%
10. Alcohol Oxidation 11%
11. Aldehydes 10%
12. Alkaloids 13%
13. Alkyl 19%
14. Alkylation 11%
15. Alkynes 11%
16. Allyl 13%
17. Amides 8%
18. Amination 8%
19. Amines 16%
20. Aryl 16%
21. Asymmetric Synthesis 23%
22. Benzene 13%
23. Biological Evaluation 9%
24. C-H Amination 19%
25. C-H Insertion 18%
26. C-H Insertion Reaction 37%
27. Carbonyl Ylide 29%
28. Carboxylate 36%
29. Catalytic Asymmetric Synthesis 12%
30. Cephalotaxine 9%
31. Chemoselective 15%
32. CIS2 10%
33. Co-oxidant 16%
34. Collidine 9%
35. Conjugate Addition 9%
36. Cycloaddition 8%
37. Diastereoselective 18%
38. Diastereoselectivity 9%
39. Diazo 39%
40. Diazoester 9%
41. Diazoketones 14%
42. Diphenyl Phosphate 9%
43. Dirhodium Complex 100%
44. Discorhabdin 10%
45. Disubstituted 10%
46. Double Bond 8%
47. Efficient Synthesis 22%
48. Enantioselectivity 52%
49. Ether 10%
50. Excellent Yields 23%
51. Furan 11%
52. Good Yield 13%
53. Hypervalent Iodine Oxidation 34%
54. Hypervalent Iodine Reagents 19%
55. Indole 18%
56. Insertion Reaction 12%
57. Intramolecular C-H Insertion 24%
58. Iodocyclization 20%
59. Keto Group 8%
60. Ketoesters 14%
61. Lactones 20%
62. Methanol 14%
63. Methyl 30%
64. Natural Products 11%
65. Opsin 8%
66. Optically Active 18%
67. Oxidative Cleavage 14%
68. Oxone 34%
69. Oxonium Ylide 23%
70. Pachastrissamine 9%
71. Percentage Yield 11%
72. Phenol Derivatives 14%
73. Phenol Oxidation 10%
74. Phenyl 11%
75. Phthaloyl Dichloride 17%
76. Polymer Support 13%
77. Quinones 23%
78. Radical Cyclization 8%
79. Radical Initiator 8%
80. Radical Reactions 9%
81. Regioselective Alkylation 10%
82. Regioselectivity 13%
83. Retinal Chromophore 8%
84. Rh(II)-catalyzed 17%
85. Rhodium(II) 19%
86. Ring-opening Cyclizations 33%
87. Room Temperature 22%
88. S-acetal 9%
89. Soluble Radical 8%
90. Spirocyclopropane 42%
91. Stereocontrolled 15%
92. Stereoselective Synthesis 29%
93. Stereoselectivity 43%
94. Styrene 9%
95. Tert 50%
96. Tetrahydrofuran 17%
97. Tetrakis 34%
98. Total Synthesis 23%
99. Trifluoroacetate 13%
100. Water-soluble 11%

Chemistry

1. 1,3-cycloaddition 16%
2. 2,2,2-trifluoroethanol 9%
3. 2,3-dihydrobenzofuran 8%
4. 3-Oxohexanoate 6%
5. Acetal 28%
6. Acetonitrile 9%
7. Acetyl 6%
8. Addition Reaction 6%
9. Alkene 15%
10. Alkyl Group 6%
11. Alkylation 17%
12. Alkyne 15%
13. Ambient Reaction Temperature 28%
14. amination 26%
15. Antitumor 6%
16. Asymmetric Synthesis 22%
17. Azide 9%
18. Baeyer-Villiger Oxidation 6%
19. Benzene 12%
20. Benzoquinone 6%
21. Boiling 6%
22. Carbonyl Compound 9%
23. Carbonyl Ylide 29%
24. Carboxamide 9%
25. Carboxylic Acid 46%
26. Catalysis 7%
27. Cephalotaxine 9%
28. Chelation 8%
29. Chemoselectivity 27%
30. Chromophore 12%
31. Cobalt 6%
32. Copolymerization 6%
33. Cycloaddition 18%
34. Cycloalkane 6%
35. cyclohexane-1,3-dione 20%
36. Cyclohexanedione 7%
37. Cyclopentane 6%
38. Cyclopentanone 6%
39. Diastereoselectivity 10%
40. Dichloromethane 11%
41. Diol 6%
42. Double Bond 9%
43. Enantioselectivity 15%
44. Ethyl 11%
45. formation 55%
46. Furan 14%
47. Hetero Diels-Alder Cycloaddition 6%
48. Heterocyclic Compound 10%
49. Hydrogen 7%
50. Hypervalence 50%
51. Immobilized Catalyst 6%
52. Immunomodulator 6%
53. Immunosuppressive Agent 6%
54. Indole 22%
55. Insertion Reaction 48%
56. Intramolecular Heck Reaction 6%
57. Iodoarene 8%
58. Ketoester 11%
59. Ketone 8%
60. Ketones 20%
61. Lactam 6%
62. Lactone 25%
63. Leucinate 28%
64. Lithium 6%
65. Methanol 14%
66. Monomer 6%
67. Myriocin 9%
68. Natural Product 17%
69. NMR Spectroscopy 9%
70. Nucleophile 15%
71. Octane 9%
72. oxidation of phenols 8%
73. Oxidative Elimination Reaction 14%
74. Oxonium Ylide 23%
75. Palladium 7%
76. Phenol 16%
77. Primary Alcohols 7%
78. Primary Amine 6%
79. Protecting Groups 8%
80. Quinone 28%
81. Radical Cyclization 8%
82. Radical Reaction 9%
83. Retinoic Acid 8%
84. Rhodium 22%
85. Ring Expansion 6%
86. Ring Opening Reaction 35%
87. Silyl Enol Ether 7%
88. Solid-State NMR 9%
89. Sphingosine 6%
90. Stereoselective Synthesis 27%
91. Stereoselectivity 14%
92. Styrene 9%
93. Sulfenylation 6%
94. Sulfonium 11%
95. Table Salt 8%
96. Tetrahydrofuran 19%
97. Thioester 6%
98. Trifluoroacetate 14%
99. Water Soluble 10%
100. Ylide 10%