分子合成化学研究室

Keyphrases

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

Chemistry

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