venkatachalam Angamuthu

Dr. venkatachalam Angamuthu

Senior Research Scientist
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 July 2019 in Organic Chemistry Frontiers
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VAvenkatachalam Angamuthu
venkatachalam Angamuthu
Faiz-Ur RahmanFaiz-Ur Rahman
Faiz-Ur Rahman
MPManuel Petroselli
Manuel Petroselli
YLYongsheng Li
Yongsheng Li
YYYang Yu
Yang Yu
JRJulius Rebek
Julius Rebek
The cavitand induced “yo-yo” motion was applied to mono-epoxidation reaction of α,ω-dienes using N -bromosuccinamide and K 2 CO 3 in D 2 O.

1 October 2015 in Applied Catalysis A: General
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VAvenkatachalam Angamuthu
venkatachalam Angamuthu
Dar-Fu TaiDar-Fu Tai
Dar-Fu Tai

14 February 2020 in Molecules
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VAvenkatachalam Angamuthu
venkatachalam Angamuthu
Dar-Fu TaiDar-Fu Tai
Dar-Fu Tai
The total synthesis of (−)-antrocin and its enantiomer are presented. Antrocin (−)-1 is an important natural product which acts as an antiproliferative agent in a metastatic breast cancer cell line (IC50: 0.6 μM). The key features of this synthesis are: (a) selective anti-addition of trimethylsilyl cyanide (TMSCN) to α,β-unsaturated ketone; (b) resolution of (±)-7 using chiral auxiliary L-dimethyl tartrate through formation of cyclic ketal diastereomers followed by simple column chromatography separation and acid hydrolysis; (c) substrate-controlled stereoselective aldol condensation of (+)-12 with monomeric formaldehyde and pyridinium chlorochromate (PCC) oxidation for synthesis of essential lactone core in (−)-14; and (d) non-basic Lombardo olefination of the carbonyl at the final step to yield (−)-antrocin. In addition, (+)-9 cyclic ketal diastereomer was converted to (+)-antrocin with similar reaction sequences.

10 February 2021 in Catalysts
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VAvenkatachalam Angamuthu
venkatachalam Angamuthu
Chia-Hung LeeChia-Hung Lee
Chia-Hung Lee
Dar-Fu TaiDar-Fu Tai
Dar-Fu Tai
Brucine diol (BD) catalyzed asymmetric Morita–Baylis–Hillman (MBH) reaction is observed for the first time. Brucine N-oxide (BNO) was found to not have an effective chiral catalyst. Faster reaction rate was obtained using unsaturated ester or aromatic aldehydes in the presence of BNO. 4-Nitrobenzaldehyde and α,β-unsaturated ketone/ester were converted to the MBH adduct in moderate yields (up to 74%) with 70% ee value by this catalytic system. The mechanism of BD catalysis is probably initiated by conjugating the vicinal diol of BD to the carbonyl group of the aromatic aldehyde through hydrogen bonding. The tertiary amine of BD acts as a nucleophile to activate vinyl ketone for coupling with the carbonyl of aldehyde through an intramolecular carbonylated reaction. Finally, the breakdown of the complex caused the formation of the MBH adduct (a benzyl-allyl alcohol). The chirality of the benzyl-allyl alcohol is likely affected by the interaction of the bulky asymmetric plane of BD.