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organic reactions and mechanisms

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RACEMIC MODIFICATION (RACEMATE || RACEMIC MIXTURE): SEPARATION OF ENANTIOMERS-RESOLUTION
An equimolar mixture of two enantiomers is called a racemic modification (or racemate or racemic mixture). When enantiomers are mixed together in equal proportion, the rotation caused by a molecule of...
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FISCHER FORMULA, FLYING WEDGE FORMULA, AND SAWHORSE FORMULA AND THEIR INTERCONVERSION
FISCHER PROJECTION FORMULA: It is a two-dimensional depiction of an organic molecule at the tetrahedral carbon center. The four bonds at the tetrahedral carbon are represented by two vertical and two...
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PART II: WEINREB KETONE SYNTHESIS: CARBON – CARBON BOND FORMATION USING WEINREB AMIDE AND ORGANOMETALLIC REAGENTS
The synthesis of ketones from N-methoxy-N-methyl amide, called as Weinreb amide, using organometallic reagents is known as the Weinreb ketone synthesis. Generally, the direct conversion of acid chlorides...
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WEINREB AMIDE SYNTHESIS: PART I: WEINREB AMIDE PREPARATION
The direct conversion of carboxylic acids or acid chlorides or esters to ketones or aldehydes using organometallic reagents usually does not result in high yield because the intermediate ketones are highly...
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MIZOROKI-HECK REACTION: CARBON-CARBON BOND FORMATION CATALYZED BY PALLADIUM
During the early 1970s Tsutomu Mizoroki and Richard F. Heck independently discovered that the reaction of aryl, benzyl, and styryl halides with alkenes at a high temperature in the presence of a hindered...
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MIGITA-KOSUGI-STILLE COUPLING: STILLE CROSS-COUPLING REACTION: CARBON-CARBON BOND FORMATION
In 1976, the first palladium-catalyzed cross-coupling of organotin compounds was accomplished by C. Eaborn, et al. The next year, M. Kosugi and T. Migita described the transition metal-catalyzed cross-coupling...
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BUCHWALD-HARTWIG CROSS-COUPLING REACTION: C-N BOND FORMATION
Aryl amines and related heterocycles are essential components in natural products, pharmaceuticals, agrochemicals, and various other compounds. This significance has driven chemists to seek advanced methods...
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WOHL-ZIEGLER BROMINATION: ALLYLIC AND BEZYLIC BROMINATION WITH N-BROMOSUCCINIMIDE (NBS)
Introducing a bromine substituent at the allylic positions of olefins or at the benzylic positions of alkylated aromatic or heteroaromatic compounds is known as the Wohl-Ziegler Bromination reaction. The...
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SUZUKI-MIYAURA CROSS-COUPLING REACTION: CARBON-CARBON BOND FORMATION
Cross-coupling reactions occur when two reagents react together with a metal catalyst to form a new covalent bond. A cross-coupling reaction in organic synthesis occurs when two fragments are joined together...
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STORK ENAMINE SYNTHESIS: ALKYLATION OF ALDEHYDE OR KETONE
An indirect method for the selective alkylation and acylation of an aldehyde or ketone is via an intermediate called ‘Enamine’. An enamine is an unsaturated compound derived from the condensation of an...
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