Create named_reactions_in_organic_synthesis.py

global_chem/global_chem/organic_synthesis/named_reactions_in_organic_synthesis.py

@@ -0,0 +1,270 @@
+#!/usr/bin/env python3
+#
+# GlobalChem - Named Reactions in Organic Synthesis
+#
+# -------------------------------------------------
+
+class NamedReactionsInOrganicSynthesis(object):
+
+  def __init__(self):
+
+      self.name = 'named_reactions_in_organic_synthesis'
+
+  @staticmethod
+  def get_smiles():
+
+      smiles = {
+        Lieben Haloform Reaction
+Benzilic Acid Rearrangement 
+Aldol Reaction
+Dieckmann Condensation
+Strecker Reation
+Hofmann Elimination
+Wiallmson Ether Synthesis 
+Cannizzaro Reaction 
+Wurtz Coulping
+Kolbe-Schmitt Reaction
+Pinacol and Semipinacol Rearrangement 
+Acyloin Condensation
+Hunsdiecker Reaction (Borodin Reaction)
+Perkin Reaction
+Glaser Coupling Reaction
+Lossen Rearrangement 
+Reimer-Tiemann Reaction
+Friedel-Crafts Acylation
+Friedel-Crafts Alkylation
+Malonic Ester Synthesis 
+Pinner Reaction
+Koenigs-Knorr Glycosidation
+Skraup and Doebner-Miller Reaction 
+Ciamician-Dennstedt Rearrangement 
+Fries-, Photo-Fries and Anionic Ortho-Fries Rearrangement 
+Hell-Volhard-Zelinsky Reaction
+Hofmann Rearrangement 
+Hantzsch Dihydropyridine Synthesis 
+Combes Quinoline Synthesis 
+Fischer Indole Synthesis 
+Hofmann–Löffler-Freytag Reaction
+Michael Addition
+von Pechmann Reaction
+Paal-Knorr Furan Synthesis
+Paal-Knorr Pyrrole Synthesis
+Sandmeyer Reaction
+Schotten-Baumann reaction
+Buchner Method of Ring Enlargement (Buchner reaction)
+Curtius Rearrangement 
+Beckman Rearrangement 
+Knorr Pyrrole Synthesis 
+Claisen Condensation/ (Claisen Reaction)
+Gabriel Synthesis 
+Japp-Klingemann Reaction 
+Reformatsky Reaction
+Tishchenko Reaction
+Dimroth Rearrangement 
+Biginelli Reaction
+Darzens Glycidic Ester Condensation
+Bischler-Napieralski Isoquinoline Synthesis
+Dienone-Phenol Rearrangement 
+Pomeranz-Fritsch Reaction
+Stobbe Condensation
+Favorskii Rearrangement and Homo-Favorskii Rearrangement 
+Knoevenagel Condensation
+Nef Reaction
+Smiles Rearrangement 
+Wacker Oxidation
+Henry Reaction
+Arbuzov Reaction (Michaelis-Arbuzov Reaction)
+Gattermann and Gattermann-Koch Formylation
+Chugaev Elimination (Xanthate Ester Pyrolysis)
+Baeyer-Villiger Oxidation/Rearrangement  
+Barbier Coupling Reaction
+Prins Reaction
+Wagner-Meerwein Rearrangement 
+Grignard Reaction
+Demjanov Rearrangement and Tiffeneau-Demjanov Rearrangement 
+Ullmann Reaction/Coupling/Biaryl Synthesis 
+Feist–Bénary Furan Synthesis 
+Wolff Rearrangement 
+Benzoin and Retro-Benzoin Condensation
+Mannich Reaction
+Nazarov Cyclization
+Ullmann Biaryl Ether and Biaryl Amine Synthesis/Condensation
+Eschweiler-Clarke Methylation
+Staudinger Ketene Cycloaddition
+Acetoacetic Ester Synthesis
+Dakin Oxidation
+Paterno-Büchi Reaction
+Prilezhaev Reaction
+Pummerer Rearrangement 
+Finkelstein Reaction
+Regitz Diazo-Transfer Reaction
+Pictet-Spengler Tetrahydroisoquinoline Synthesis 
+Wolff-Kishner Reduction
+Madelung Indole Synthesis
+Claisen Rearrangement 
+Clemmensen Reduction 
+Wharton Olefin Synthesis (Wharton Transposition)
+Chichibabin Amination Reaction (Chichibabin Reaction)
+Ferrier Reaction/Ferrier Rearrangement 
+Houben-Hoesch Reaction/Synthesis 
+Aza-Wittig Reaction
+Meisenheimer Rearrangement 
+Staudinger Reaction
+Wittig Reaction
+Wohl-Ziegler Bromination
+Passerini Multicomponent Reaction
+Meyer-Schuster and Rupe Rearrangement 
+Schmidt Reaction
+Amadori Reaction/Rearrangement 
+Meerwein-Ponndorf-Verley Reduction
+Stephen Aldehyde Synthesis
+Diels-Alder Cycloaddition 
+Neber Rearrangement 
+Balz-Schiemann Reaction (Schiemann Reaction)
+Dakin-West Reaction
+Stevens Rearrangement 
+Nenitzescu Indole Synthesis
+Criegee Oxidation
+Riley Selenium Dioxide Oxidation
+Baker-Venkataraman Rearrangement 
+Prévost Reaction 
+Arndt-Eistert Homologation/Synthesis
+Payne Rearrangement 
+Robinson Annulation
+Claisen-Ireland Rearrangement 
+Oppenauer Oxidation
+Sommelet-Hauser Rearrangement 
+Meerwin Arylation
+Quasi-Favorskii Rearrangement 
+Snieckus Directed Ortho Metalation
+Carrol Rerrangement (Kimel-Cope Rearrangement)
+Cope Rearrangement 
+Ramberg–Bäcklund Rearrangement 
+Wittig-[1,2]- and [2,3]-Rearrangement
+Alder (Ene) Reaction
+Hetero Diels-Alder Reaction (HDA)
+Birch Reduction
+Jones Oxidation/Oxidation of Alcohols by Chromium Reagents 
+Peterson Olefination
+Ritter Reaction
+Cope Elimination/(Cope Reaction)
+Cornforth Rearrangement 
+Bamford-Stevens-Shapiro Olefination
+Grob Fragmentation
+Wharton Fragmentation
+Stork Enamine Synthesis
+Alkene (Olefin) Metathesis
+Brown Hydroboration Reaction
+Kornblum Oxidation
+Brook Rearrangement 
+Doering-LaFlamme Allene Synthesis
+Horner-Wadsworth-Emmons Olefination 
+Simmons-Smith Cyclopropanation
+Heine Reaction
+Ugi Multicomponent Reaction
+Vilsmeier-Haack Formylation
+Vinylcyclopropane-Cyclopetene Rearrangement 
+Barton Nitrile Ester Reaction
+Kröhnke Pyridine Synthesis
+Barton Radical Decarboxylation Reaction
+Corey-Chaykovsky Epoxidation and Cyclopropanation
+DeMayo Cycloaddition (Enone-Alkene [2+2] Photocycloaddition
+Nagata Hydrocyanation Reaction
+Castro-Stevens Coupling
+Corey-Winter Olefination
+Pfitzner-Moffatt Oxidation
+Eschenmoser-Claisen Rearrangement 
+Oxy-Cope Rearrangement/Anionic Oxy-Cope Rearrangement 
+Tsuji-Trost Reaction (Allylation)
+Tsuji-Wilkinson Decarbonylation
+Wittig Reaction- Schlosser Modification
+Aza-Claisen Rearrangement (3-Aza-Cope Rearrangement)
+Aza-Cope Rearrangement
+Eschenmoser-Tanabe Fragmentation
+Krapcho Dealkoxycarbonylation
+Mitsunobo Reaction
+Seyferth-Gilber Homologation
+Baylis-Hillman Reaction
+Heck Reaction
+Minisci Reaction
+Mislow-Evans Rearrangement 
+Prins-Pinacol Rearrangement
+Schwartz Hydrozirconation
+Burgess Dehydration Reaction
+Johnson-Claisen Rearrangement
+Aza-[2,3]-Wittig Rearrangement 
+Corey-Kim Oxidation
+Eschenmoser Methenylation
+Hajos-Parrish Reaction
+Nicholas Reaction
+Bergman Cycloaromatization Reaction
+Corey-Fuchs Alkyne Synthesis
+Kumada Cross Coupling Reaction
+McMurry Coupling
+Saegusa Oxidation
+Julia-Lythgoe Olefination
+Mukaiyama Aldol Reaction
+Pauson-Khand Reaction
+Pinnick Oxidation
+Polonovski Reaction
+Stetter Reaction
+Overman Rearrangement 
+Alkyne Metathesis
+Corey-Nicolau Macrolactonization
+Danishefsky's Diene Cycloaddition
+Rubottom Oxidation
+Swern Oxidation
+Barton-McCombie Radical Deoxygenation Reaction
+ Dötz Benzannulation Reaction
+Sonogashira Cross-Coupling
+Enders SAMP/RAMP Hydrazone Alkylation
+Negishi Cross-Coupling
+Sakurai Allylation
+Stille Cross-Coupling (Migita-Kosugi-Stille Coupling)
+Tebbe Olefination/Petasis-Tebbe Olefination
+Davis Oxaziridine Oxidation
+Nozaki-Hiyama-Kishi Coupling 
+Bartoli Indole Synthesis
+Luche Reduction
+Roush Asymmetric Allylation
+Midland Alpine Borane Reduction
+Suzuki Cross-Coupling (Suzuki-Miyaura Cross-Coupling)
+Yamaguchi Macrolactonization
+Kagan-Molander Samarium-Diiodide Coupling
+Noyori Asymmetric Hydrogenation
+Sharpless Asymmetric Dihydroxylation Reaction
+Sharpless Asymmetric Epoxidation Reaction
+Corey-Bakashi-Shibata (CBS) Reduction
+Danheiser Cyclopenten Annulation
+Evans Aldol Reaction
+Weinreb Ketone Synthesis
+Buchwald-Hartwig Cross-Coupling
+Dess-Martin Oxidation
+Fleming-Tamao Oxidation
+Horner-Wadsworth-Emmons Olefination (Still-Gennari modification)
+Danheiser Benzannulation
+Stille Carbonylative Cross-Couping
+Enyne Metathesis
+Keck Macrolactonization
+Ley Oxidation
+Takai-Utimoto Olefination (Takai Reaction)
+Stille-Kelly Coupling
+Kahne Glycosidation
+Kulinkovich Reaction
+Jacobsen-Katsuki Epoxidation
+Larock Indole Synthesis
+Keck Asymmetric Allylation
+Keck Radical Allylation
+Petasis Boronic Acid-Mannich Reaction
+Myers Asymmetric Alkylation
+Smith-Tietze Multicomponent Dithiane Linchpin Coupling 
+Jacobsen Hydrolytic Kinetic Resolution of Epoxides 
+Miyaura Boration Reaction
+Petasis-Ferrier Rearrangement
+Sharpless Asymmetric Aminohydroxylation Reaction
+Shi Asymmetric Epoxidation
+      }
+
+      return smiles
+
+