The Prins reaction 1 is often related to the Kriewitz reaction. 2 The latter leads to unsaturated
alcohol 1 from a-pinene and formaldehyde through a thermal 'ene-rearrangement'(Eq. 1) …

The Wittig reaction involves the synthesis of an alkene via the conversion of an aldehyde or
ketone with the already generated ylide from a phosphonium salt. Significantly, when this …

(–)-Isopulegol undergoes Prins cyclization reaction in the presence of 20 wt% of acid-treated
montmorillonite K10 to produce octahydro-2H-chromen-4-ols in good yields and with high …

A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via
Prins cyclization - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & …

Rhizopus arrhizus mediated bioreduction was optimized using acetophenone as a model
substrate. Various parameters such as bio-processing conditions, reaction time, substrate …

Total synthesis of (+/−)-diospongin A via Prins reaction - ScienceDirect Skip to main contentSkip
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Diverse array of biopolymers and second metabolites (particularly polyketide natural
products) has been manufactured in nature through an enzymatic iterative assembly of …

The natural products having tetrahydropyran unit with multiple chiral centers serve as
magnificent building blocks for various active pharmaceutical ingredients (APIs).'Prins …

For the last ten years our group has been working toward the development of an asymmetric
hydration approach to polyketide natural products based on the regioselective hydration of …

Stereoselective total synthesis of decarestrictine-J via Ring Closing Metathesis (RCM) -
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