Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sagar S Thorat"'
Publikováno v:
ACS Omega, Vol 3, Iss 6, Pp 7036-7045 (2018)
Externí odkaz:
https://doaj.org/article/70d016236fba4b2fb72086c7689cceca
Autor:
Ashwini K. Nakate, Sagar S. Thorat, Shailja Jain, Gamidi Rama Krishna, Kumar Vanka, Ravindar Kontham
Publikováno v:
Organic Chemistry Frontiers. 9:802-809
An unprecedented Ag(i)-catalyzed [3 + 3]-annulation of alkynyl alcohols (5-hexyn-1-ols) and α,β-unsaturated ketones is reported to construct simple to complex chromanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70700c8d23c21e75bd68cb4069d0aaf5
https://doi.org/10.1039/d1qo01643a
https://doi.org/10.1039/d1qo01643a
Publikováno v:
The Journal of Organic Chemistry. 86:13572-13582
A full account of our efforts toward the stereoselective total synthesis of sesquiterpenoid-derived natural products (±)-pleurospiroketals A and B is described. Commercially available 3-methyl-2-cyclohexenone and 2,2-dimethyloxirane were used as key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecfd2047afda5c15c4aad21fdd7487c2
https://doi.org/10.1021/acs.joc.1c01634
https://doi.org/10.1021/acs.joc.1c01634
Autor:
Ravindar Kontham, Sagar S Thorat
Publikováno v:
Organic Chemistry Frontiers. 8:2110-2162
The furo-pyranone framework is widely present in the molecular structure of various biologically potent natural products and un-natural small molecules, and it represents a valuable target in synthetic organic chemistry and medicinal chemistry. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d609a8ecb9fc65ec467a45fc1fede782
https://doi.org/10.1039/d0qo01421d
https://doi.org/10.1039/d0qo01421d
Autor:
Yash Mankad, Sagar S. Thorat, Pronay Das, Gamidi Rama Krishna, Ravindar Kontham, D. Srinivasa Reddy
Publikováno v:
The Journal of organic chemistry. 87(5)
This work showcases an unprecedented Au(III)-catalyzed cascade cyclization of 2-(4-hydroxyalkynyl)benzoates to access benzannulated [5,5]-oxaspirolactones related to biologically active natural products. This reaction proceeds through an initial 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3795d0f8baeda2d3455b11e93f9e4d5
https://pubmed.ncbi.nlm.nih.gov/35188770
https://pubmed.ncbi.nlm.nih.gov/35188770
Publikováno v:
Organic Letters. 20:872-875
Ag(I)- or Ag(I)-Au(I)-catalyzed cascade annulation of alkynols (5-hexyn-1-ol systems) with α-ketoesters involving a dual activation process (π and σ) has been developed for the first time. This reaction proceeds through cycloisomerization of alkyn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1883fe058178d9f91756a2dcbb8e029
https://doi.org/10.1021/acs.orglett.7b04027
https://doi.org/10.1021/acs.orglett.7b04027
Autor:
Sagar S. Thorat, Ravindar Kontham
Publikováno v:
Organicbiomolecular chemistry. 17(31)
Oxaspirolactones are ubiquitous structural motifs found in natural products and synthetic molecules with a diverse biochemical and physicochemical profile, and represent a valuable target in natural product chemistry and medicinal chemistry. Since th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23de949d0b95ffe4312b1ef502e6d026
https://pubmed.ncbi.nlm.nih.gov/31313792
https://pubmed.ncbi.nlm.nih.gov/31313792
Autor:
Madhukar Shivaji Pratapure, Digambar A. Kambale, Rajesh G. Gonnade, Ravindar Kontham, Sagar S Thorat
Publikováno v:
Chemical communications (Cambridge, England). 53(49)
A novel Lewis acid catalyzed intermolecular cascade annulation of alkynols with α-ketoesters has been developed. This simple and efficient cascade annulation proceeds through a 5-exo-dig cyclization of alkynols followed by annulation with α-ketoest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6792e742c766fe496e579b8537cdfd5b
https://pubmed.ncbi.nlm.nih.gov/28585651
https://pubmed.ncbi.nlm.nih.gov/28585651
Publikováno v:
Journal of Sol-Gel Science and Technology
Journal of Sol-Gel Science and Technology, Springer Verlag, 2017, 81 (3), pp.791-796. ⟨10.1007/s10971-016-4244-4⟩
Journal of Sol-Gel Science and Technology, Springer Verlag, 2017, 81 (3), pp.791-796. ⟨10.1007/s10971-016-4244-4⟩
Biomaterials and wettability have played a crucial role in the biocompatibility with a host matrix of body fluid and cells. We discuss designing superhydrophobic biomaterials for novel applications such as temporally implant, contact lenses, controll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4bba0311e00f8b950adcda323fe55ae
https://hal.archives-ouvertes.fr/hal-02489584
https://hal.archives-ouvertes.fr/hal-02489584
Autor:
F. Pedraza, Vinayak G. Parale, B. P. Relekar, G. M. Lohar, Sagar S. Thorat, Satish A. Mahadik
Publikováno v:
Journal of Sol-Gel Science and Technology
Journal of Sol-Gel Science and Technology, Springer Verlag, 2016, 78 (3), pp.475-481. ⟨10.1007/s10971-016-3974-7⟩
Journal of Sol-Gel Science and Technology, Springer Verlag, 2016, 78 (3), pp.475-481. ⟨10.1007/s10971-016-3974-7⟩
The binary superhydrophobic–superhydrophilic surface has been successfully achieved by a combination of nanoscale texture roughness on micro-textured cotton thread network by layer-by-layer deposition method through the single-step sol–gel route.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55305d6e596cdbfe9225213aaed04120
https://hal.archives-ouvertes.fr/hal-02488997
https://hal.archives-ouvertes.fr/hal-02488997