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I. Namboothiri - One of the best experts on this subject based on the ideXlab platform.
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SAEGUSA Enone Synthesis to SZARVASY–SCHÖPF Carbomethoxylation
Organic Syntheses Based on Name Reactions, 2012Co-Authors: Alfred Hassner, I. NamboothiriAbstract:This article contains brief overviews, mechanisms and practical details for organic synthesis named reactions and processes beginning with the letter ‘S’. Reactions included in this section are: SAEGUSA Enone Synthesis; SAKURAI Allylation via Allylsilanes; SANDMEYER Isatin Synthesis; SANDMEYER–GATTERMANN Aromatic Substitution; SANGER Amino Acid Labeling Reagent; SARETT Cr Oxidizing Reagent; SCHEINER Aziridine Triazoline Synthesis; SCHENCK Allylic Oxidation; SCHIEMANN Aromatic Fluorination; SCHMIDT Rearrangement via Azides; SCHMITZ Diaziridine Synthesis; SCHOLL Polyaromatic Synthesis; SCHOLLKOPF Amino Acid Synthesis; SCHOLLKOPF–BARTON–ZARD Pyrrole Synthesis; SCHOLTZ Indolizine Synthesis; SCHOTTEN–BAUMANN Alcohol and Amine Acylation; SCHWARTZ Hydrozirconation; SCHWEIZER Allylamine Synthesis; SCHWEIZER Allenyl Azine Rearrangement; SCHWESINGER Phosphazene Bases; SEEBACH Chiral Oxazolidinones; SEEBACH–BECK TADDOL Reagent; SEEBACH–COREY Dithiane Reagents; SEMMLER–WOLFF Oxime Aromatization; SEYFERTH Acyllithium Reagent; SEYFERTH Dihalocarbene Reagent; SEYFERTH – GILBERT Diazoalkane Reagent; SHAPIRO Olefination via Tosylhydrazones; SHARPLESS Allylic Amination; SHARPLESS Asymmetric Dihydroxylation; SHARPLESS Asymmetric Epoxidation; SHEEHAN Carbodiimide Coupling Reagent; SHERADSKY – ENDO Hetero-Cope Rearrangement; SHESTAKOV Hydrazino Acid Synthesis; SHEVERDINA–KOCHESHKOV Electrophilic Amination; SHIBASAKI Ti–N Complex; SIEGRIST Stilbene Synthesis; SIMCHEN Azaheterocycle Synthesis; SIMMONS – SMITH Cyclopropanation; SIMONIS Benzopyrone Synthesis; SKATTEBOL Vinyldihalocyclopropane Rearrangement; SKRAUP Quinoline Synthesis; SMILES Aromatic Rearrangement; SMITH–MIDDLETON–ROZEN Fluorination; SNIECKUS Carbamate Rearrangement; SODERQUIST Boranes; SOMMELET Aldehyde Synthesis; SOMMELET Ammonium Ylide Rearrangement; SONN – MULLER Aldehyde Synthesis; SONOGASHIRA Acetylene Coupling; SOULA Phase Transfer Catalyst; SPECKAMP Acyliminium Ions; SPENGLER–PFANNENSTIEL Sugar Oxidation; SREBNIK–QUNTAR Cyclopropyl Phosphonates; STAAB Carbonylimidazole; STAUDINGER Azide Reduction; STAUDINGER Ketene Cycloadditions; STAUDINGER – PFENNINGER Thiirane Dioxide Synthesis; STEGLICH – HASSNER Direct Alcohol Esterification; STEPHEN Aldehyde Synthesis; STEPHENS–CASTRO Acetylene Coupling; STETTER 1,4-Dicarbonyl Synthesis; STEVENS Ammonium Ylide Rearrangement; STIEGLITZ N -Haloamine Rearrangement; STILES–SISTI Grignard Formylation; STILLE Carbonyl Synthesis; STILLE Cross Coupling; STILL–GENNARI Z-Olefin Synthesis; STOBBE Succinic Ester Condensation; STOLTZ Asymmetric Ketone α-Allylation; STORK–HUNIG Cyanohydrin Alkylation; STORK Enamine Alkylation; STORK Radical Cyclization; STORK Reductive Cyclization; STORK–HAUSER Aminonitrile Alkylation; STORK–ZHAO Z -Iodo-olefin Synthesis; STORY Macrocycle Synthesis; STRECKER Aminoacid Synthesis; Stryker Regioselective Reduction; SUAREZ Photochemical lodo Functionalization; SUZUKI Aromatic Nitration; SUZUKI Selective Nitrile Reduction; SUZUKI–MIYAURA C C Coupling; SWARTS Fluoroalkane Synthesis; SWERN Alcohol Oxidation; SZARVASY–SCHOPF Carbomethoxylation
Alfred Hassner - One of the best experts on this subject based on the ideXlab platform.
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SAEGUSA Enone Synthesis to SZARVASY–SCHÖPF Carbomethoxylation
Organic Syntheses Based on Name Reactions, 2012Co-Authors: Alfred Hassner, I. NamboothiriAbstract:This article contains brief overviews, mechanisms and practical details for organic synthesis named reactions and processes beginning with the letter ‘S’. Reactions included in this section are: SAEGUSA Enone Synthesis; SAKURAI Allylation via Allylsilanes; SANDMEYER Isatin Synthesis; SANDMEYER–GATTERMANN Aromatic Substitution; SANGER Amino Acid Labeling Reagent; SARETT Cr Oxidizing Reagent; SCHEINER Aziridine Triazoline Synthesis; SCHENCK Allylic Oxidation; SCHIEMANN Aromatic Fluorination; SCHMIDT Rearrangement via Azides; SCHMITZ Diaziridine Synthesis; SCHOLL Polyaromatic Synthesis; SCHOLLKOPF Amino Acid Synthesis; SCHOLLKOPF–BARTON–ZARD Pyrrole Synthesis; SCHOLTZ Indolizine Synthesis; SCHOTTEN–BAUMANN Alcohol and Amine Acylation; SCHWARTZ Hydrozirconation; SCHWEIZER Allylamine Synthesis; SCHWEIZER Allenyl Azine Rearrangement; SCHWESINGER Phosphazene Bases; SEEBACH Chiral Oxazolidinones; SEEBACH–BECK TADDOL Reagent; SEEBACH–COREY Dithiane Reagents; SEMMLER–WOLFF Oxime Aromatization; SEYFERTH Acyllithium Reagent; SEYFERTH Dihalocarbene Reagent; SEYFERTH – GILBERT Diazoalkane Reagent; SHAPIRO Olefination via Tosylhydrazones; SHARPLESS Allylic Amination; SHARPLESS Asymmetric Dihydroxylation; SHARPLESS Asymmetric Epoxidation; SHEEHAN Carbodiimide Coupling Reagent; SHERADSKY – ENDO Hetero-Cope Rearrangement; SHESTAKOV Hydrazino Acid Synthesis; SHEVERDINA–KOCHESHKOV Electrophilic Amination; SHIBASAKI Ti–N Complex; SIEGRIST Stilbene Synthesis; SIMCHEN Azaheterocycle Synthesis; SIMMONS – SMITH Cyclopropanation; SIMONIS Benzopyrone Synthesis; SKATTEBOL Vinyldihalocyclopropane Rearrangement; SKRAUP Quinoline Synthesis; SMILES Aromatic Rearrangement; SMITH–MIDDLETON–ROZEN Fluorination; SNIECKUS Carbamate Rearrangement; SODERQUIST Boranes; SOMMELET Aldehyde Synthesis; SOMMELET Ammonium Ylide Rearrangement; SONN – MULLER Aldehyde Synthesis; SONOGASHIRA Acetylene Coupling; SOULA Phase Transfer Catalyst; SPECKAMP Acyliminium Ions; SPENGLER–PFANNENSTIEL Sugar Oxidation; SREBNIK–QUNTAR Cyclopropyl Phosphonates; STAAB Carbonylimidazole; STAUDINGER Azide Reduction; STAUDINGER Ketene Cycloadditions; STAUDINGER – PFENNINGER Thiirane Dioxide Synthesis; STEGLICH – HASSNER Direct Alcohol Esterification; STEPHEN Aldehyde Synthesis; STEPHENS–CASTRO Acetylene Coupling; STETTER 1,4-Dicarbonyl Synthesis; STEVENS Ammonium Ylide Rearrangement; STIEGLITZ N -Haloamine Rearrangement; STILES–SISTI Grignard Formylation; STILLE Carbonyl Synthesis; STILLE Cross Coupling; STILL–GENNARI Z-Olefin Synthesis; STOBBE Succinic Ester Condensation; STOLTZ Asymmetric Ketone α-Allylation; STORK–HUNIG Cyanohydrin Alkylation; STORK Enamine Alkylation; STORK Radical Cyclization; STORK Reductive Cyclization; STORK–HAUSER Aminonitrile Alkylation; STORK–ZHAO Z -Iodo-olefin Synthesis; STORY Macrocycle Synthesis; STRECKER Aminoacid Synthesis; Stryker Regioselective Reduction; SUAREZ Photochemical lodo Functionalization; SUZUKI Aromatic Nitration; SUZUKI Selective Nitrile Reduction; SUZUKI–MIYAURA C C Coupling; SWARTS Fluoroalkane Synthesis; SWERN Alcohol Oxidation; SZARVASY–SCHOPF Carbomethoxylation
