Deep Eutectic Solvent Promoted Regioselective Synthesis of Densely Functionalized Mono and Bisindolylalkenes from
            β
            ‐Ketodithioesters

Thokchom Jeeta Devi; Thokchom Prasanta Singh; Rajkumar Romeshkumar Singh; Elangbam Holender Singh; Okram Mukherjee Singh

doi:10.1002/slct.202003779

Deep Eutectic Solvent Promoted Regioselective Synthesis of Densely Functionalized Mono and Bisindolylalkenes from β ‐Ketodithioesters

ChemistrySelect ◽

10.1002/slct.202003779 ◽

2020 ◽

Vol 5 (42) ◽

pp. 13351-13357

Author(s):

Thokchom Jeeta Devi ◽

Thokchom Prasanta Singh ◽

Rajkumar Romeshkumar Singh ◽

Elangbam Holender Singh ◽

Okram Mukherjee Singh

Keyword(s):

Deep Eutectic Solvent ◽

Regioselective Synthesis

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ChemInform Abstract: Deep Eutectic Solvent: A Simple, Environmentally Benign Reaction Media for Regioselective Synthesis of 2,3,4-Trisubstituted 1H-Pyrroles.

ChemInform ◽

10.1002/chin.201535126 ◽

2015 ◽

Vol 46 (35) ◽

pp. no-no

Author(s):

Hanuman P. Kalmode ◽

Kamlesh S. Vadagaonkar ◽

Kaliyappan Murugan ◽

Sattey Prakash ◽

Atul C. Chaskar

Keyword(s):

Deep Eutectic Solvent ◽

Regioselective Synthesis ◽

Environmentally Benign ◽

Reaction Media

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Deep Eutectic Solvent‐Mediated Regioselective Synthesis of Imidazoheterocycles

Macromolecular Symposia ◽

10.1002/masy.202100089 ◽

2021 ◽

Vol 400 (1) ◽

pp. 2100089

Author(s):

Dattatray B. Yedage ◽

Dattatray V. Patil

Keyword(s):

Deep Eutectic Solvent ◽

Regioselective Synthesis

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Deep eutectic solvent: a simple, environmentally benign reaction media for regioselective synthesis of 2,3,4-trisubstituted 1H-pyrroles

RSC Advances ◽

10.1039/c5ra03270a ◽

2015 ◽

Vol 5 (44) ◽

pp. 35166-35174 ◽

Cited By ~ 23

Author(s):

Hanuman P. Kalmode ◽

Kamlesh S. Vadagaonkar ◽

Kaliyappan Murugan ◽

Sattey Prakash ◽

Atul C. Chaskar

Keyword(s):

Deep Eutectic Solvent ◽

Regioselective Synthesis ◽

Environmentally Benign ◽

Highly Efficient ◽

Reaction Media

A greener, rapid and highly efficient synthetic protocol for the construction of pyrroles has been achieved.

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Recovery of metabolites from natural deep eutectic solvent matrices by countercurrent separation

Planta Medica ◽

10.1055/s-0035-1556494 ◽

2015 ◽

Vol 81 (11) ◽

Author(s):

Y Liu ◽

J Garzon ◽

JB Friesen ◽

DC Lankin ◽

JB McAlpine ◽

...

Keyword(s):

Deep Eutectic Solvent ◽

Natural Deep Eutectic Solvent

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2-O-Acyl-3-O-(1-Acyloxyalkyl) Prodrugs of 5,6-Isopropylidene-L-Ascorbic Acid and L-Ascorbic Acid: Regioselective Synthesis, Antioxidant Activity, and Ability to Permeate Silicone Membranes

10.26226/morressier.57d6b2b5d462b8028d88ddf1 ◽

2016 ◽

Author(s):

Kenneth Sloan

Keyword(s):

Antioxidant Activity ◽

Ascorbic Acid ◽

Regioselective Synthesis ◽

Silicone Membranes

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OnePot Regioselective Synthesis of Heterocyclic Compounds by the Application of Sonogashira Reaction as One of the Steps: A Review

Journal of Chemistry and Chemical Sciences ◽

10.29055/jccs/576 ◽

2018 ◽

Vol 8 (2) ◽

pp. 212-230

Author(s):

Sanjay Nath

Keyword(s):

Heterocyclic Compounds ◽

Regioselective Synthesis ◽

Sonogashira Reaction ◽

One Pot

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Evaluation of microemulsions containing a large amount of a deep eutectic solvent as a potential transdermal carrier of resveratrol

Japanese Journal of Applied Physics ◽

10.35848/1347-4065/abaa94 ◽

2020 ◽

Vol 59 (9) ◽

pp. 095004

Author(s):

Mina Sakuragi ◽

Reina Yano ◽

Sabrina Binti Mohamed Hasnol ◽

Katsuki Kusakabe

Keyword(s):

Deep Eutectic Solvent

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Facile Regioselective Synthesis of Pyrrolo-Pyrones: Tandem Reaction of 4- N-(4 -Aryloxy-2 -ynyl), N-Methyl Pyran-2-Ones with 3-Chloroperoxybenzoic Acid (Experimental Section)

Letters in Organic Chemistry ◽

10.2174/157017805774717580 ◽

2005 ◽

Vol 2 (8) ◽

pp. 739-741 ◽

Cited By ~ 1

Author(s):

Krishna Majumdar ◽

Habibur Rahaman ◽

Brindaban Roy

Keyword(s):

Regioselective Synthesis ◽

Tandem Reaction ◽

Experimental Section

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Regioselective Synthesis of Functionalized Oxime Ethers

Letters in Organic Chemistry ◽

10.2174/157017810791824874 ◽

2010 ◽

Vol 7 (6) ◽

pp. 479-482 ◽

Cited By ~ 5

Author(s):

Jun Liu ◽

Dafeng Li ◽

Jian Li ◽

Chunju Li ◽

Xueshun Jia

Keyword(s):

Regioselective Synthesis

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Regioselective Synthesis of 2-Chloroquinoline Based Ethyl 4-(3- Hydroxyphenyl)-2,7,7-Trimethyl-5-Oxo-1,4,5,6,7,8-Hexahydroquinoline-3- Carboxylates and their In-Silico Evaluation Against P. falciparum Lactate Dehydrogenase

Medicinal Chemistry ◽

10.2174/1573406411666150430132055 ◽

2015 ◽

Vol 11 (8) ◽

pp. 789-797

Author(s):

Kancherla Rajesh ◽

Pandian Lavanya ◽

Pethaperumal Iniyavan ◽

Sundaramoorthy Sarveswari ◽

Sudha Ramaiah ◽

...

Keyword(s):

Lactate Dehydrogenase ◽

In Silico ◽

Regioselective Synthesis

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Deep Eutectic Solvent Promoted Regioselective Synthesis of Densely Functionalized Mono and Bisindolylalkenes from β ‐Ketodithioesters

ChemInform Abstract: Deep Eutectic Solvent: A Simple, Environmentally Benign Reaction Media for Regioselective Synthesis of 2,3,4-Trisubstituted 1H-Pyrroles.

Deep Eutectic Solvent‐Mediated Regioselective Synthesis of Imidazoheterocycles

Deep eutectic solvent: a simple, environmentally benign reaction media for regioselective synthesis of 2,3,4-trisubstituted 1H-pyrroles

Recovery of metabolites from natural deep eutectic solvent matrices by countercurrent separation

2-O-Acyl-3-O-(1-Acyloxyalkyl) Prodrugs of 5,6-Isopropylidene-L-Ascorbic Acid and L-Ascorbic Acid: Regioselective Synthesis, Antioxidant Activity, and Ability to Permeate Silicone Membranes

OnePot Regioselective Synthesis of Heterocyclic Compounds by the Application of Sonogashira Reaction as One of the Steps: A Review

Evaluation of microemulsions containing a large amount of a deep eutectic solvent as a potential transdermal carrier of resveratrol

Facile Regioselective Synthesis of Pyrrolo-Pyrones: Tandem Reaction of 4- N-(4 -Aryloxy-2 -ynyl), N-Methyl Pyran-2-Ones with 3-Chloroperoxybenzoic Acid (Experimental Section)

Regioselective Synthesis of Functionalized Oxime Ethers

Regioselective Synthesis of 2-Chloroquinoline Based Ethyl 4-(3- Hydroxyphenyl)-2,7,7-Trimethyl-5-Oxo-1,4,5,6,7,8-Hexahydroquinoline-3- Carboxylates and their In-Silico Evaluation Against P. falciparum Lactate Dehydrogenase

OnePot Regioselective Synthesis of Heterocyclic Compounds by the Application of Sonogashira Reaction as One of the Steps: A Review