Chemodivergent Reactions of Aromatic Ring-Annulated Hexahydrocyclopentafurans with Various Aldehydes
TJ Kindala, K Yano, K Takatori, M Mizukami… - Organic …, 2024 - ACS Publications
Hexahydro-2 H-cyclopenta [b] furan fused to electron-rich aromatic rings reacts with various
aromatic aldehydes in different modes to build diverse frameworks. The reaction of a …
aromatic aldehydes in different modes to build diverse frameworks. The reaction of a …
Transition metal/Lewis acid catalyzed reactions of zerumbone for diverse molecular motifs
M Biji, B Prabha, RS Lankalapalli… - The Chemical …, 2021 - Wiley Online Library
Zerumbone is a naturally occurring humulene type sesquiterpene, isolated from the
rhizomes of Zingiber zerumbet (L.) Smith with excellent therapeutic potential and is …
rhizomes of Zingiber zerumbet (L.) Smith with excellent therapeutic potential and is …
Cascade Aza-Prins/Friedel–Crafts Reaction of Homocinnamyloxycarbamate and Aromatic Aldehydes Yielding Aromatic Ring-Annulated Hydrocyclopenta-1, 2 …
TJ Kindala, K Takatori, S Nagumo - The Journal of Organic …, 2025 - ACS Publications
The cascade aza-Prins/Friedel–Crafts reaction of homocinnamyloxycarbamate with electron-
rich aromatic aldehydes has been successfully established. Most of the aromatic aldehydes …
rich aromatic aldehydes has been successfully established. Most of the aromatic aldehydes …
Enantioselective Synthesis of a Furan Lignan (+)-Sylvone
E Lee, J Bang, J Kwon, CM Yu - The Journal of Organic Chemistry, 2015 - ACS Publications
A synthesis of natural tetrahydrofuran lignan (+)-sylvone is achieved starting from methyl
allenoate in 5 steps. The synthesis begins from an enantioselective aldol reaction of methyl …
allenoate in 5 steps. The synthesis begins from an enantioselective aldol reaction of methyl …
Substitution dependent stereoselective construction of bicyclic lactones and its application to the total synthesis of pyranopyran, tetraketide and polyrhacitide A
BVS Reddy, DO Biradar, YV Reddy… - Organic & …, 2016 - pubs.rsc.org
A novel bicyclization strategy has been developed for the stereoselective synthesis of
bicyclic lactones, ie 7-aryl or alkyl-2, 6-dioxabicyclo [3.3. 1] nonan-3-ones through a domino …
bicyclic lactones, ie 7-aryl or alkyl-2, 6-dioxabicyclo [3.3. 1] nonan-3-ones through a domino …
Prins Cyclization: Novel Strategy towards the Diastereoselective Total Synthesis of (–)-Cryptocaryolone
DO Biradar, YD Mane, JS Yadav, BVS Reddy - Synthesis, 2023 - thieme-connect.com
A highly diastereoselective total synthesis of TBDPS-protected (–)-cryptocaryolone has been
achieved in 12 linear steps with an overall yield of 7.1%, following a recently developed …
achieved in 12 linear steps with an overall yield of 7.1%, following a recently developed …
Tandem Prins/Wagner/Ritter process for the stereoselective synthesis of (3-oxabicyclo [4.2. 0] octanyl) amide and (1-(5-aryltetrahydrofuran-3-yl) cyclobutyl) amide …
BVS Reddy, K Muralikrishna, JS Yadav… - Organic & …, 2015 - pubs.rsc.org
Three-component coupling of aldehydes, vinylcyclopropyl carbinols, and nitriles in the
presence of 10 mol% TMSOTf at− 40 to 0° C in dichloromethane affords a novel class of (3 …
presence of 10 mol% TMSOTf at− 40 to 0° C in dichloromethane affords a novel class of (3 …
Tandem Prins Cyclization for the Stereoselective Synthesis of the 4,5‐Diaryl‐hexahydropyrano[3,4‐c]chromene Skeleton of Calyxins I and J
A Prins bicyclization strategy for the stereoselective synthesis of trans‐fused
hexahydropyrano [3, 4‐c] chromene derivatives in good to excellent yields has been …
hexahydropyrano [3, 4‐c] chromene derivatives in good to excellent yields has been …
A novel domino cyclization for the stereoselective synthesis of indeno [2, 1-c] pyran and cyclopenta [c] pyran derivatives
BVS Reddy, NP Raju, B Someswarao… - Organic & …, 2015 - pubs.rsc.org
A novel bicyclization of 2-(2-(hydroxymethyl)-1-methylene-2, 3-dihydro-1H-inden-2-yl)
ethanol with aldehydes in the presence of 10 mol% BF3· OEt2 in dichloromethane at 0–25° …
ethanol with aldehydes in the presence of 10 mol% BF3· OEt2 in dichloromethane at 0–25° …
Prins‐Driven Friedel–Crafts Reaction for the Stereoselective Synthesis of Hexahydroindeno[2,1‐c]pyran Derivatives
A strategy has been devised for the stereoselective synthesis of hexahydroindeno [2, 1‐c]
pyran scaffolds through a domino cyclization of (E)‐3, 5‐diphenylpent‐4‐en‐1‐ol with …
pyran scaffolds through a domino cyclization of (E)‐3, 5‐diphenylpent‐4‐en‐1‐ol with …