Datasets:

hcaoaf commited on
Commit
4cc0425
·
verified ·
1 Parent(s): 5aa28c1

Upload taxonomy_rxn_types.json

Browse files
Files changed (1) hide show
  1. taxonomy_rxn_types.json +97 -0
taxonomy_rxn_types.json ADDED
@@ -0,0 +1,97 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ {
2
+ "Carbon-Carbon_Bond_Formation": [
3
+ "Chloro Suzuki coupling",
4
+ "Iodo Miyaura boration",
5
+ "Grignard ester substitution",
6
+ "Bromo Miyaura boration",
7
+ "Chloro Miyaura boration",
8
+ "Claisen-Schmidt condensation",
9
+ "Bromo Stille reaction",
10
+ "Knoevenagel condensation",
11
+ "Triflyloxy Sonogashira coupling",
12
+ "Triflyloxy Miyaura boration",
13
+ "Bromo Sonogashira coupling",
14
+ "Chloro Sonogashira coupling",
15
+ "Iodo Suzuki coupling",
16
+ "Grignard + acid chloride ketone synthesis",
17
+ "Bromo Grignard reaction",
18
+ "Iodo Grignard reaction",
19
+ "Iodo Stille reaction",
20
+ "Friedel-Crafts acylation",
21
+ "Keto alpha-alkylation",
22
+ "Bromo Suzuki coupling",
23
+ "Iodo Sonogashira coupling",
24
+ "Weinreb ketone synthesis",
25
+ "Wittig olefination",
26
+ "Chloro Grignard reaction",
27
+ "Chloro Stille reaction"
28
+ ],
29
+ "Carbon-Heteroatom_Bond_Formation": [
30
+ "Esterification",
31
+ "Iodo N-methylation",
32
+ "Mesyloxy N-alkylation",
33
+ "Mitsunobu imide reaction",
34
+ "N-Cbz protection",
35
+ "Weinreb amide synthesis",
36
+ "Ester Schotten-Baumann",
37
+ "Iodo N-alkylation",
38
+ "Williamson ether synthesis",
39
+ "Bromo Buchwald-Hartwig amination",
40
+ "Mitsunobu ester synthesis",
41
+ "Mitsunobu aryl ether synthesis",
42
+ "Carboxy to carbamoyl",
43
+ "Alcohol + amine condensation",
44
+ "Chloro N-alkylation",
45
+ "Amide Schotten-Baumann",
46
+ "Bromo N-alkylation",
47
+ "Fischer-Speier esterification",
48
+ "Steglich esterification",
49
+ "Methyl esterification",
50
+ "Iodo Buchwald-Hartwig amination",
51
+ "Carbamate Schotten-Baumann",
52
+ "Sulfonic ester Schotten-Baumann",
53
+ "Carboxylic acid + amine condensation",
54
+ "Mitsunobu sulfonamide reaction",
55
+ "N-Boc protection",
56
+ "Sulfonamide Schotten-Baumann",
57
+ "Chloro Buchwald-Hartwig amination"
58
+ ],
59
+ "Deprotection_Reactions": [
60
+ "CO2H-Et deprotection",
61
+ "Ester hydrolysis",
62
+ "O-TBS deprotection",
63
+ "N-Boc deprotection",
64
+ "O-TBDPS deprotection",
65
+ "CO2H-Me deprotection",
66
+ "N-Cbz deprotection",
67
+ "O-Bn deprotection",
68
+ "O-TIPS deprotection",
69
+ "CO2H-tBu deprotection"
70
+ ],
71
+ "Functional_Group_Interconversion": [
72
+ "Iodination",
73
+ "Hydroxy to chloro",
74
+ "Ketone to alcohol reduction",
75
+ "Chlorination",
76
+ "Methoxy to hydroxy",
77
+ "Aldehyde Dess-Martin oxidation",
78
+ "Wohl-Ziegler bromination",
79
+ "Bechamp reduction",
80
+ "Carboxylic ester + amine reaction",
81
+ "Bromination",
82
+ "Bromo Grignard preparation",
83
+ "Ketone Dess-Martin oxidation",
84
+ "Aldehyde reductive amination",
85
+ "Sulfanyl to sulfonyl",
86
+ "Darzens bromination",
87
+ "SNAr ether synthesis",
88
+ "Ketone reductive amination",
89
+ "Darzens chlorination",
90
+ "Ester to alcohol reduction"
91
+ ],
92
+ "Other_Reactions": [
93
+ "Isocyanate + alcohol reaction",
94
+ "Isocyanate + amine urea coupling",
95
+ "Pinner reaction"
96
+ ]
97
+ }