0.8 beta
34k Abbreviations for chemists (brows the MOBILE EDITION) .
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Name Reactions
Ugi four-component reaction

Vilsmeier-Haack reaction

Hock rearrangement

Chichibabin pyridine synthesis

Betti reaction

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Doebner reaction

Clemmensen reduction

McMurry reaction

Conrad-Limpach synthesis

Cadiot-Chodkiewicz coupling

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JC
Johnson–Claisen

BZ
Barton-Zard

Hantzsch pyrrole synthesis

Pictet-Spengler reaction

CBS
Corey-Bakshi-Shibata reduction

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Buchwald-Hartwig amination

Freund reaction

Kabachnik-Fields reaction

McFadyen-Stevens reaction

NKR
Newman-Kwart rearrangement

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NHK
Nozaki-Himaya-Kishi reaction

Tebbe olefination

Hammick reaction

Einhorn–Brunner reaction

MBH
Morita-Baylis-Hillman

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Wittig reaction

Feist-Benary synthesis

HWE
Horner-Wadsworth-Emmons

Bamford-Stevens reaction

Algar-Flynn-Oyamada reaction

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Madelung synthesis

Paal-Knorr synthesis

Barton reaction

Robinson annulation

Michaelis-Arbuzov reaction

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Pomeranz-Fritsch reaction

PKR
Pauson-Khand reaction

Meerwein-Ponndorf-Verley reduction

Pauson–Khand reaction

Baeyer-Drewson indigo synthesis

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MPV
Meerwein-Ponndorf-Verley reduction

Reimer–Tiemann reaction

Mizoroki-Heck reaction

Blanc chloromethylation

Horner-Wadsworth-Emmons reaction

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Japp-Maitland condensation

Kornblum oxidation

Meyer-Schuster rearrangement

Blaise reaction

Morita-Baylis-Hillman reaction

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Auwers synthesis

Bouveault aldehyde synthesis

Oppenauer oxidation

Hosomi-Sakurai reaction

Dutt-Wormall reaction

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Forster-Decker method

Abramovitch-Shapiro tryptamine synthesis

Hunsdiecker reaction

Mukaiyama aldol addition

Fukuyama coupling

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Baeyer-Villiger oxidation

Swern oxidation

Dieckmann condensation

Kostanecki acylation

Hiyama coupling

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Yamaguchi esterification

Stetter reaction

BZ
Belousov-Zhabotinsky

Balz–Schiemann reaction

Gattermann-Koch reaction

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FTS
Fischer-Tropsch synthesis

Menshutkin reaction

Graebe-Ullmann reaction

Appel reaction

MKS
Migita-Kosugi-Stille coupling

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3,3-dimethyl-1-(trifluoromethyl)-1,2-benziodoxole [887144-97-0]

Prévost reaction

Sonogashira coupling

MH
Mizoroki-Heck reaction

Borsche–Drechsel cyclization

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Cope rearrangement

Cope reaction

Newman-Kwart rearrangement

Julia olefination

Migita-Kosugi-Stille coupling

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Nozaki-Himaya-Kishi reaction

Simmons-Smith reaction

Negishi coupling

Whiting reaction

Angeli-Rimini reaction

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Reed reaction

Pfitzinger reaction

Alder-ene reaction

Tsuji–Trost reaction

PK
Pauson-Khand

-----

Corey-Bakshi-Shibata reduction [-]

Barton–Zard synthesis

Elbs persulfate oxidation

Elbs reaction

Gabriel synthesis

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Ritter reaction

Kumada coupling

Adams decarboxylation

Arndt–Eistert reaction

Kolbe-Schmitt reaction [-]

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Herz reaction

Chugaev elimination

samarium(II) iodide [32248-43-4]

Biginelli reaction

Perkow reaction

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RS
Rochelle salt [304-59-6]

MAR
Mukaiyama aldol reaction

Smiles rearrangement

FC
Friedel-Crafts

Reformatsky reaction

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MA
Michael addition

MA
Michaelis–Arbuzov

MR
Michael reaction

SMC
Suzuki-Miyaura coupling

Corey-Fuchs reaction

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SAE
Sharpless asymmetric epoxidation

LS
Liebeskind-Srogl coupling

HM
Heck-Matsuda reaction

Ugi
Ugi reaction

Dess-Martin oxidation

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Schotten-Baumann reaction

Piers-Rubinsztajn reaction

DA
Diels-Alder

Kumada catalyst-transfer polycondensation

FBW
Fritsch-Buttenberg-Wiechell

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Heck-Matsuda reaction

Schwartz′s reagent [37342-97-5]

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