Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Yogesh D. Mane"'
Publikováno v:
SynOpen, Vol 06, Iss 04, Pp 312-318 (2022)
A concise and diastereoselective total synthesis of tetraketide and euscapholide is described in ten steps in 10.6% overall yield from acetaldehyde and (S)-pent-4-ene-1,2-diol. Jacobsen hydrolytic kinetic resolution, Prins cyclization, ring-closing
Externí odkaz:
https://doaj.org/article/fb2fdddb24a74b2c86a21c3f28aacdba
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100717- (2023)
A concise and facile diastereoselective first total synthesis of bicyclic styryl lactone 1 is described in nine steps. This biologically active bicyclic styryl lactone was obtained in 8% overall yield from cinnamaldehyde 2 and (R)-3-hydroxyhex-5-enoi
Externí odkaz:
https://doaj.org/article/70bd0e82bd44412caa7dec1675eab750
Publikováno v:
Journal of Chemistry, Vol 2013 (2013)
The present paper introduces a simple and efficient method for the synthesis of substituted benzimidazoles by heterocyclization of different o-phenylenediamines and substituted aromatic carboxylic acid/aldehyde in the presence of zirconyl nitrate as
Externí odkaz:
https://doaj.org/article/98fb0ebb3d3041aab87aa715b4c9e711
Publikováno v:
SynOpen. :312-318
A concise and diastereoselective total synthesis of tetraketide and euscapholide is described in ten steps in 10.6% overall yield from acetaldehyde and (S)-pent-4-ene-1,2-diol. Jacobsen hydrolytic kinetic resolution, Prins cyclization, ring-closing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::310cdfca73f7c5588e0f92d574acc40b
https://doi.org/10.1055/s-0042-1751381
https://doi.org/10.1055/s-0042-1751381
Autor:
Vandana A. Gaikwad, Radhakrishnan M. Tigote, Subiya K. Kazi, Rahul M. Khobragade, Yogesh D. Mane, Appasaheb W. Suryawanshi
AlX.YB2O3 [(6-X-Y)P2O5]. TeO3 (X = 3, 2, 1, and Y = 2.5, 1.5, and 0.5) were sintered for 2 hours at 800°C using the sol-gel method. The ultraviolet-visible study shows maximum absorbance at 264 nm with optical band gap energy range of 4.21 to 4.24 e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc71c1c7f898e6b907b2e19525bda62
https://doi.org/10.21203/rs.3.rs-2819437/v1
https://doi.org/10.21203/rs.3.rs-2819437/v1
Autor:
Vishal G. More, Dinesh N. Nadimetla, Geeta A. Zalmi, Vilas K. Gawade, Ratan W. Jadhav, Yogesh D. Mane, Sheshanath V. Bhosale
Publikováno v:
ChemistryOpen
The Front Cover shows a core‐substituted naphthalene diimide with dimethylamine (DDPT) groups which has been used as a reversible acid‐base sensor. The color‐changing tides of the sea represent the acid‐base‐mediated colorimetric changes th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db806618e35dfc643b70b9438a2f3c5a
https://doi.org/10.1002/open.202200142
https://doi.org/10.1002/open.202200142
Autor:
Vishal G. More, Dinesh N. Nadimetla, Geeta A. Zalmi, Vilas K. Gawade, Ratan W. Jadhav, Yogesh D. Mane, Sheshanath V. Bhosale
Publikováno v:
ChemistryOpen. 11
A new 'Off-On' system designed and synthesised by functionalisation of a naphthalene diimide (NDI) core with dimethylamine produces 4,9-bis(dimethylamino)-2,7-dioctylbenzo[lmn][3,8]-phenanthroline-1,3,6,8-(2H,7H)-tetraone, abbreviated as DDPT (1). DD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80cd65b2714e5c4b64af469c8ff93721
https://doi.org/10.1002/open.202200060
https://doi.org/10.1002/open.202200060
Publikováno v:
Tetrahedron. 132:133242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed075e9758353e185173718c11e63133
https://doi.org/10.1016/j.tet.2022.133242
https://doi.org/10.1016/j.tet.2022.133242
Publikováno v:
Journal of Heterocyclic Chemistry. 57:724-730
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45e4ec86c6e301b0a9d857e3503bd9a4
https://doi.org/10.1002/jhet.3812
https://doi.org/10.1002/jhet.3812
Publikováno v:
Journal of Heterocyclic Chemistry. 56:1111-1116
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e693d3dabde50df182ba65b967190bc
https://doi.org/10.1002/jhet.3500
https://doi.org/10.1002/jhet.3500