Search Results - "Pattanayak, Manas R."

Strain‐Promoted 1,3‐Dithiolium‐4‐olates–Alkyne Cycloaddition by Kumar, Ramar Arun, Pattanayak, Manas R., Yen‐Pon, Expédite, Eliyan, Jijy, Porte, Karine, Bernard, Sabrina, Riomet, Margaux, Thuéry, Pierre, Audisio, Davide, Taran, Frédéric

“…Reported here is the reactivity of mesoionic 1,3‐dithiolium‐4‐olates towards strained alkynes, leading to thiophene cycloaddition products. In the process, the…”
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Iodocyclization and Prins-Type Macrocyclization: An Efficient Formal Synthesis of Leucascandrolide A by Yadav, J. S, Pattanayak, Manas R, Das, Pragna P, Mohapatra, Debendra K

“…The formal total synthesis of leucascandrolide A has been achieved in 20 steps from a known epoxide with an overall yield of 11.5% following a recently…”
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Total Synthesis of Myceliothermophins C, D, and E by Nicolaou, K. C., Shi, Lei, Lu, Min, Pattanayak, Manas R., Shah, Akshay A., Ioannidou, Heraklidia A., Lamani, Manjunath

“…The total synthesis of cytotoxic polyketides myceliothermophins E (1), C (2), and D (3) through a cascade‐based cyclization to form the trans‐fused decalin…”
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Protecting-Group Directed Stereoselective Intramolecular Nozaki-Hiyama-Kishi Reaction: A Concise and Efficient Total Synthesis of Amphidinolactone A by Mohapatra, Debendra K., Das, Pragna P., Pattanayak, Manas R., Gayatri, Gaddamanugu, Sastry, G. Narahari, Yadav, J. S.

“…A convergent total synthesis of amphidinolactone A, a cytotoxic macrolide from the cultured dinoflagellate Amphidinium sp., is described in 13 linear steps…”
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Total Synthesis of Thailanstatin A by Nicolaou, K. C, Rhoades, Derek, Lamani, Manjunath, Pattanayak, Manas R, Kumar, S. Mothish

“…The total synthesis of the spliceosome inhibitor thailanstatin A has been achieved in a longest linear sequence of nine steps from readily available starting…”
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Streamlined Total Synthesis of Uncialamycin and Its Application to the Synthesis of Designed Analogues for Biological Investigations by Nicolaou, K. C, Wang, Yanping, Lu, Min, Mandal, Debashis, Pattanayak, Manas R, Yu, Ruocheng, Shah, Akshay A, Chen, Jason S, Zhang, Hongjun, Crawford, James J, Pasunoori, Laxman, Poudel, Yam B, Chowdari, Naidu S, Pan, Chin, Nazeer, Ayesha, Gangwar, Sanjeev, Vite, Gregory, Pitsinos, Emmanuel N

“…From the enediyne class of antitumor antibiotics, uncialamycin is among the rarest and most potent, yet one of the structurally simpler, making it attractive…”
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Total Synthesis of MyceliothermophinsC, D, and E by Nicolaou, K C, Shi, Lei, Lu, Min, Pattanayak, Manas R, Shah, Akshay A, Ioannidou, Heraklidia A, Lamani, Manjunath

“…The total synthesis of cytotoxic polyketides myceliothermophinsE (1), C (2), and D (3) through a cascade-based cyclization to form the trans-fused decalin…”
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Strain‐Promoted 1,3‐Dithiolium‐4‐olates–Alkyne Cycloaddition by Kumar, Ramar Arun, Pattanayak, Manas R., Yen‐Pon, Expédite, Eliyan, Jijy, Porte, Karine, Bernard, Sabrina, Riomet, Margaux, Thuéry, Pierre, Audisio, Davide, Taran, Frédéric

“…Reported here is the reactivity of mesoionic 1,3‐dithiolium‐4‐olates towards strained alkynes, leading to thiophene cycloaddition products. In the process, the…”
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Ring-closing metathesis (RCM) based synthesis of the macrolactone core of amphidinolactone A by Mohapatra, Debendra K, Pattanayak, Manas R, Das, Pragna P, Pradhan, Tapas R, Yadav, J S

“…A convergent synthesis of the macrolactone core of amphidinolactone A has been achieved, in a 10 step linear sequence with 32% overall yield, through a…”
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Protecting-Group Directed Stereoselective Intramolecular Nozaki-Hiyama-Kishi Reaction: A Concise and Efficient Total Synthesis of Amphidinolactone A (Eur. J. Org. Chem. 25/2010) by Mohapatra, Debendra K., Das, Pragna P., Pattanayak, Manas R., Gayatri, Gaddamanugu, Sastry, G. Narahari, Yadav, J. S.

“…The cover picture shows shows how a bulky protecting group directs the intramolecular Nozaki–Hiyama–Kishi reaction to afford exclusively one stereoisomer,…”
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Total Synthesis of Myceliothermophins C, D, and E by Nicolaou, K. C., Shi, Lei, Lu, Min, Pattanayak, Manas R., Shah, Akshay A., Ioannidou, Heraklidia A., Lamani, Manjunath

“…The total synthesis of cytotoxic polyketides myceliothermophins E (1), C (2), and D (3) through a cascade‐based cyclization to form the trans‐fused decalin…”
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Total Synthesis of MyceliothermophinsC, D, and E by Nicolaou, K C, Shi, Lei, Lu, Min, Pattanayak, Manas R, Shah, Akshay A, Ioannidou, Heraklidia A, Lamani, Manjunath

“…The total synthesis of cytotoxic polyketides myceliothermophinsE (1), C (2), and D (3) through a cascade-based cyclization to form the trans-fused decalin…”
Get full text