MITS has secured NIRF India Ranking 2024 in the band 201 to 300.
Dr. Vishnumaya Bisai

Qualification : Ph.D. (IIT, Kanpur)

Designation : Assoc. Professor

Details of Educational Qualification:

Course Specialization Group College Name/University Year of Passing
Ph.D. Organic Chemistry Organic Chemistry IIT Kanpur 2009
M.Sc. Chemistry M.Sc. DDU Gorakhpur University 2002
B.Sc. Chemistry, Physics & Mathematics B.Sc. DDU Gorakhpur University 2000

 

List of Publications

S.No Title of the Paper Full Details of Journal Name / Conference Name, Volume number, page number, Date
1 Asymmetric total syntheses of (–)-ar-turmerone, (–)-dihydro-ar-turmerone, (–)-ar-dehydrocurcumene, and (–)-ar-himachalene via a key allylic oxidative rearrangement Tetrahedron Lett. 2021, 73, 153105)
2 Concise asymmetric total syntheses of (−)-nuciferol, (−)-nuciferal, and (−)-dihydrocurcumene via Rh(I)-catalyzed boronic acid addition Tetrahedron Lett. 2021, 65, 152790)
3 Catalytic Asymmetric Total Syntheses of (+)--Cuparenone, (+)-Cuparene and (+)-Herbertene Tetrahedron Lett. 2020, 61,152169)
4 Formal Total Syntheses of (+)‐ and (–)‐ar‐Macrocarpene via Rh(I)‐BINAP Catalyzed Conjugate Addition Eur. J. Org. Chem. 2020, 2435)
5 Catalytic enantioselective total synthesis of (−)-ar-Tenuifolene Tetrahedron Lett. 2020, 61, 151850)
6 Catalytic asymmetric total syntheses of sesquiterpenoids, (+)- and (−)-ar-macrocarpene Tetrahedron 2020, 76, 130918)
7 Concise total syntheses of (+)- and (−)-ar-macrocarpene Tetrahedron Lett. 2020, 61, 151736)
8 Total Synthesis of (+)-ar-Macrocarpene Org. Biomol. Chem. 2019, 17, 7140)
9 Unified approach to the sesquiterpenoids, lauranes and cyclolauranes: Total Synthesis of (±)-Isolaurene Tetrahedron Lett. 2019, 60, 150941)
10 A unified approach to sesquiterpenes sharing trimethyl(p-tolyl) cyclopentanes: Formal total synthesis of (±)-laurokamurene B Tetrahedron Lett. 2019, 60, 2039)
11 Invited Review: Biosynthetic Relationships and Total Syntheses of Naturally Occurring Benzo[c]phenanthridine Alkaloids Asian J. Org. Chem. 2019, 57, 946)
12 Invited Review: Diels-Alder Reactions in Creating Complexity in Higher Order Isoprenoids: Proposed Biosynthesis and Biomimetic Total Syntheses Asian J. Org. Chem. 2018, 56, 1488)
13 Book Chapter: “Protecting-Group-Free Synthesis of Complex Natural Products and Analogues” John Wiley and Sons Publishers, Edited by Prof. Rodney A.Fernandes, IIT Bombay
14 Invited Review: 'Naturally Occurring Taiwaniaquinoids: Biosynthetic Relationships and Synthetic Approaches ARKIVOC, 2018, VI, 57)
15 Invited Review: Recent Development on Asymmetric Alkynylations Tetrahedron Lett. 2016, 57, 4771)
16 Approach to Isoindolinones, Isoquinolinones, and THIQs via Lewis Acid-Catalyzed Domino Strecker- Lactamization/Alkylations Org.Lett. 2016, 18, 634)
17 Asymmetric Syntheses of Medicinally Important Isoindolinones, (S)-PD 172938, (R)-JM 1232 and Related Structures J. Org. Chem. 2016, 81, 4779)
18 Ni(II)-Catalyzed Highly Stereo- and Regioselective Syntheses of Isoindolinones and Isoquinolinones from in Situ Prepared Aldimines Triggered by Homoallylation/Lactamization Cascade Org. Lett. 2015, 17, 5650).
19 Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama- Mannich Lactamization Alkylations: Application in the Synthesis of Homolaudanosine Org. Lett. 2015, 17, 2780).
20 An Efficient Entry to syn- and anti-Selective Isoindolinones via Organocatalytic Direct Mannich/Lactamization Sequence Org. Lett. 2015, 17, 2102.
21 Asymmetric Alkynylation/Lactamization Cascade: An Expeditious Entry to Enantioenriched Isoindolinones Featured in: Yamamoto and Furukawa Synfacts 2014, 10, 1298 and “ChemInform Abstracts, Wiley-VCH, 2015, DOI: 10.1002/chin.201512169.”
22 A General Catalytic Route to Isoindolinones and Tetrahydroisoquinolines: Application in the Synthesis of Crispine A Featured in: “ChemInform Abstracts, Wiley-VCH, 2015, DOI: 10.1002/chin.201519076”
23 Invited E-ROS: Encyclopedia for Reagents in Organic Synthesis (EROS) on "Benzenecarboperoxoic acid, 1,1-dimethylethyl Ester" published by John and Wiley & Sons Ltd. 2012 (RN01616).
24 Review: Organocatalytic Asymmetric Vinylogous Aldol Reaction ( Featured in “ChemInform Abstracts, Wiley-VCH, 2012, 28, 251.
25 Invited Review: Small Molecule Catalyzed Asymmetric Aldol Reaction Featured in: “ChemInform Abstracts, Wiley-VCH, 2012, DOI: 10.1002/chin.201240243.
26 Methoxypyridines in the Synthesis of Lycopodium Alkaloids: Total Synthesis of (±)-Lycoposerramine R Featured in “ChemInform Abstracts, Wiley-VCH, 2009,43, 74.
27 Highly Enantioselective Water-Compatible Diamine Organocatalyst for Asymmetric Aldol Reaction Featured in “ChemInform Abstracts, Wiley-VCH, 2011, 27, 63.
28 Highly Efficient Small Organic molecules for Enantioselective Direct Aldol reaction in Organic and Aqueous Media Featured in: Downer-Relay and Jackson Annu. Rep. Prog. Chem., Sect. B 2011,107, 157-181. NIH Public Access, June 4, 2011.
29 Highly Enantioselective Organocatalytic Direct Aldol Reaction in an Aqueous Medium Featured in: List and Stadler Synfacts 2007, 8, 0875. Popularized as Singh’s Catalyst by Berkessel et al. in Org. Process Res. Dev. 2012, 16, 123. Berkesselet al. J. Am. Chem. Soc. 2012, 134, 11196.
30 Highly Enantioselective Water-Compatible Organocatalyst for Michael Reaction of Ketones to Nitro- olefins Featured in: List and Pan Synfacts 2007, 5, 0538.
31 Highly Enantioselective Organocatalytic Direct Aldol Reaction Catalyzed by Organic Molecules Featured in “ChemInform Abstracts, Wiley-VCH, 2007, 03, 26.