Name Reactions by Our Heros

A:   Amphiphile-2nd Generation WZQ
Allylation Reactions-ZGS

B:     Buchwald-Hartwig-LFK  
Bestmann-Ohira Reagent

C:    COPE ELIMINATION(COPE REACTION)
COPE REARRANGEMENT-ZL
CBS REDUCTION
COREY-CHAYKOVSKY EPOXIDATION AND CYCLOPROPANATION-LYG
COREY-FUCHS ALKYNE SYNTHESIS-ZL
Corey-Nicolaou macrolactonization-ZPT
COREY-WINTER OLEFINATION-CPH
Cornforth rearrangement-WZQ
Criegee oxidation-LYG
Curtius_Rearrangement-SZM
Catellani reaction-GYD

D:   DAKIN-WEST REACTION-CPH
Dakin oxidation-ZL
DANISHEFSKY’S DIENE CYCLOADDITION-LYG
DANHEISER CYCLOPENTENE ANNULATION-WZQ
Davis oxaziridine oxidations-SYZ
DE MAYO CYCLOADDITION-LFK
DESS-MARTIN OXIDATION
Demjanov rearrangement reaction
DIELS-ALDER CYCLOADDITION-LYG
DIECKMANN CONDENSATION-WZQ
DOERING-LAFLAMME ALLENE SYNTHESIS-syz
Dimroth Rearragement-YGH
Dyotropic Reactions-CPH

E:     ENDERS SAMPRAMP HYDRAZONE ALKYLATION-ZL
Enyne metathesis-SYZ
ESCHENMOSER METHENYLATION-CPH
Eschenmoser-Tanabe-CLR
ESCHENMOSER-CLAISEN REARRANGEMENT-WZQ
Evans aldol-LYG
ESCHWEILER-CLARKE METHYLATION-ZL

F:     Ferrier reaction-rearrangement-CLR
Finkelstein reaction-LML
FRIEDEL-Crafts acylation-LYG
FLEMING-TAMAO OXIDATION-ZL
FRIES-REARRANGEMENT-SYZ
Friedel-Crafts Alkylation-YGH
Aromatic Finkelstein Reaction-LML

G:     GATTERMANN AND GATTERMANN-KOCH FORMYLATION-LML
GRIGNARD REACTION-LLJ
GLASER COUPLING-ZGS
Grob Fragmentation-ZL

H:   Hajos-Parrish reaction YGH
HANTZSCH DIHYDROPYRIDINE SYNTHESIS-CPH
Heck Reaction-HZF
Hell-Volhard Zelinsky-LML
Henry Reaction-ZGS
HETERO DIELS-ALDER CYCLOADDITION-WT
HOFMANN ELIMINATION-SYZ
HofmannLöffler-Freytag reaction (HLF reaction)-CPH
Hofmann rearrangement-HZF
Horner–Wadsworth–Emmons reaction-WZQ
HOUBEN-HOESCH REACTION-WT
HUNSDIECKER REACTION-ZL

I:   Isoquinoline Synthesis-LLM

J:      JOHNSON-CLAISEN REARRANGEMENT-CPH
Japp-Klingemann reaction-LLM
JULIA-LYTHGOE OLEFINATION-HZF
JONES OXIDATION-WEL
JACOBSEN-KATSUKI EPOXIDATION-SYZ

K:     Kahne glycosidation-LML
KNOEVENAGEL CONDENSATION-ZL
KNORR PYRROLE SYNTHESIS-wt
KOLBE-SCHMITT REACTION-ZL
Krapcho dealkoxycarbonylation-SYZ
KORNBLUM OXIDATION-LLM
Kröhnke pyridine synthesis-HZF
Kumada crossing-coupling-LML
Kulinkovich
L:     LIEBEN HALOFORM REACTION-ZL
Lossen rearrangement-SYZ
LUCHE REDUCTION-HZF
LAROCK INDOLE SYNTHESIS-WT

M:   Mcmurry coupling-LML
Meerwein reduction-20160517-LHJ
Meerwein reduction-ZGS
MEYER-SCHUSTER AND RUPE REARRANGEMENT-WT
MEISENHEIMER REARRANGEMENT-ZL Meisenheimer rearrangement-ZMJ
Midland Alpine-Borane reduction-SYZ
Miniscireaction-CPH
Mislow-evans rearrangement-HZF
Mitsunobu Reaction wzq
MIYAURA BORATION-Zhou Guanshen
MUKAIYAMA ALDOL REACTION-SYZ
MYERS ASYMMETRIC ALKYLATION-CPH
MEYER-SCHUSTER AND RUPE REARRANGEMENT-ZMJ
Meyer-Schuster rearrangement-SYX

N:    Nagata Hydrocyanation-HZF
Neber rearrangement-LML
NEF REACTION-ZGS
NICHOLAS REACTION-ZL
NAZAROV Reaction wzq
NHK reaction-CPH
Noyori asymmetric hydrogenation-HZF

O:    Oppenauner oxidation wzq
Overman rearrangement-LML
OVERMAN REARRANGEMENT-YHT

P:   PASSERINI MULTICOMPONENT REACTION-ZL
Paal–Knorr synthesis-LLM
PATERNO-BüCHI REACTION-ZGS
Perkin reaction-CPH
Payne-HZF
PETASIS BORONIC ACID-MANNICH REACTION wzq
PETERSON OLEFINATION-ZL
PINACOL AND SEMIPINACOL REARRANGEMENT-CJR
PINNER REACTION-ZGS
Polonovski-HZF
PINNICK OXIDATION-CPH
PRÉVOST REACTION-LML
Prins Reaction-ZGS
PUMMERER REARRANGEMENT-HZF
PAAL-KNORR FURAN SYNTHESIS
Paal-Knorr Pyrrole Synthesis-LML
PAUSON-KHAND REACTION-LXL
PAYNE REARRANGEMENT-YC

R:     Ramberg-Backbuld rearrangement-LML
Reformatsky Reaction-LLM
REGITZ DIAZO TRANSFER-ZL
Riley Oxidation-ZGS
Ritter Reaction-LML
ROBINSON ANNULATION-ZGS
REIMER-TIEMANN REACTION-CJR
RAMBERG-BÄCKLUND REARRANGEMENT-SX
Reformatsky reaction-GYD
REGITZ DIAZO TRANSFER-YHT
REIMER-TIEMANN REACTION-LML
Riley oxidation wzq
Ritter reaction
Robinson annulation-LXL
Roush asymmetric allylation-ZL
Rubottom-CX

S:     SAEGUSA OXIDATION-wzq
SAEGUSA OXIDATION-LLM
SAKURAI ALLYLATION -HWL
Sandmeyer Reaction-LXL
Schmidt reaction-ZL
SCHOTTEN-BAUMANN REACTION-ZGS
Seyferth-Gilbert homologation-GYD
SIMMONS-SMITH CYCLOPROPANATION-SX
Skraup and Doebner-Miller quinoline synthesis-GYD
SMILES REARRANGEMENT-LML
Smith-Tietze coupling
SNIECKUS DIRECTED ORTHO METALATION-CPH
Sommelet–Hauser rearrangement wzq
Sonogashira-SYZ
Standinger Reaction-LXL
STEPHEN ALDEHYDE SYNTHESIS-YC
Stetter Reaction-ZY
STRECKER REACTION-ZL
Steven Rearrangement-WY
STILLE CROSS-COUPLING-WXQ
STORK ENAMINE SYNTHESIS-ZMJ
SAEGUSA OXIDATION-SX
Stobbe condensation–GL

T:

TAKAI REACTION-SX

TEBBE OLEFINATION-GYD

Tishchenko reaction-lml

TSUJI-TROST REACTION-YHT

U:

UGI MULTICOMPONENT REACTION-WZQ

Ullmann Coupling Reaction-SYZ

V:

Vinylcyclopropane-cyclopentene-YC

Von Pechmann Reaction-WY

W:

WILKINSON’S CATALYST-CPH

Wacker Oxidation-XQW

 

Name reaction from Chinese contributors:

Chanrearrangement-LG

ROSKAMPFENG REACTION-SYX

WOLFF-KISHNER-HUANG REDUCTION-BSL

Hou Te-Pang Solvay Process-chenpeihao

Lu-[3+2]-cycloaddition reaction

Lu-Trost-Inoue reaction,

Ullmann-Ma reaction/Ma-Buchwald-Hartwig Amination

Shi Epoxidation

Norrish-Yang Photocyclization

Zhang Enyne Cycloisomerization

Stork-Zhao Olefination

……

To be updated by all our Chinese chemists…..

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