Contenu connexe
Similaire à Heterocyclic compounds _ Organic Chemistry _ B. Pharm. (13)
Heterocyclic compounds _ Organic Chemistry _ B. Pharm.
- 117. 2018
P Y R I D I N E
Synthesis
1. Hantzsch pyridine synthesis
117
- 118. 2018
P Y R I D I N E
Synthesis
1. Hantzsch pyridine synthesis
118
- 119. 2018
P Y R I D I N E
Synthesis
1. Hantzsch pyridine synthesis
119
- 120. 2018
P Y R I D I N E
Synthesis
2. The Guareschi Synthesis
120
- 121. 2018
P Y R I D I N E
Synthesis
3. From 1,5 - Dicarbonyl Compounds
121
- 122. 2018
P Y R I D I N E
Synthesis
4. From Oxazoles Kondrat'eva pyridine synthesis
122
- 125. 2018
P Y R I D I N E
C2
C3
C4
Reactions
2. Electrophilic substitution to C
125
- 126. 2018
P Y R I D I N E
Reactions
2. Electrophilic substitution to C
126
- 127. 2018
P Y R I D I N E
Reactions
2. Electrophilic substitution to C
127
- 128. 2018
P Y R I D I N E
Reactions
3. Nucleophilic substitution
Why pyridine undergoes nucleophilic substitution
reaction at 2-position.
128
C3
C2
- 129. 2018
P Y R I D I N E
Reactions
3. Nucleophilic substitution
129
- 130. 2018
P Y R I D I N E
Reactions
4. Pyridine as Nucleophilic catalyst
130
- 131. 2018
P Y R I D I N E
Reactions
5. Reduction
131
- 137. A Z E P I N E S
2018
Synthesis
1. Valence-bond Isomerization
137
- 138. A Z E P I N E S
2018
Synthesis
2. From Phenylazide
138
- 139. A Z E P I N E S
2018
Synthesis
3. From Nitrobenzene
139
- 140. A Z E P I N E S
2018
Reactions
140
- 141. A Z E P I N E S
2018
Reactions
3. Diels-Alder reaction
- 6+2 π electron reaction
141
- 142. A Z E P I N E S
2018
Medicinal Uses
142
- 146. 2018
Q U I N O L I N E
Synthesis
1. Skraup Quinoline synthesis
146
- 150. 2018
Q U I N O L I N E
Reactions
2. Electrophilic aromatic substitution
150
- 153. 2018
Q U I N O L I N E
Reactions
5. Nucleophilic substitution
153
- 160. 2018
I S O Q U I N O L I N E
Reactions
1. Electrophilic addition to N
160
- 161. 2018
I S O Q U I N O L I N E
Reactions
2. Electrophilic aromatic substitution
161
- 162. 2018
I S O Q U I N O L I N E
Reactions
3. Reduction reactions
162
- 163. 2018
I S O Q U I N O L I N E
Reactions
4. Oxidation
163
- 164. 2018
I S O Q U I N O L I N E
Reactions
5. Nucleophilic substitution
164
- 165. 2018
I S O Q U I N O L I N E
Medicinal uses
165
- 166. 2018
I S O Q U I N O L I N E
Medicinal uses
166
- 171. 2018
A C R I D I N E
Reactions
2. Electrophilic aromatic substitution
171
- 172. 2018
A C R I D I N E
Reactions
3. Reduction reactions
172
- 173. 2018
A C R I D I N E
Reactions
4. Oxidation
173
- 174. 2018
A C R I D I N E
Reactions
5. Nucleophilic substitution
174
- 177. 2018
I N D O L E
Synthesis
1. Fischer indole synthesis
177
- 178. 2018
I N D O L E
Synthesis
1. Fischer indole synthesis
Mechanism
178
- 179. 2018
I N D O L E
Synthesis
1. Fischer indole synthesis
Mechanism
179
- 180. 2018
I N D O L E
Synthesis
1. Fischer indole synthesis
180
- 181. 2018
I N D O L E
Synthesis
2. Bischler–Möhlau indole synthesis
181
- 182. 2018
I N D O L E
Synthesis
3. Madelung synthesis
182
- 183. 2018
I N D O L E
Synthesis
3. Madelung synthesis
E.g.
183
- 214. 2018
P U R I N E
Reactions
2. Electrophilic aromatic substitution
214
- 215. 2018
P U R I N E
Reactions
3. Nucleophilic substitution
215
Notes de l'éditeur
- In a heterocyclic ring, other things being equal, numbering preferably commences at a saturated rather than at an unsaturated hetero atom
- https://www.synarchive.com/named-reactions/hantzsch-thiazole-synthesis