Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Bhawani S. Joshi"'
Autor:
Alok K. Verma, Priti Khemaria, Jyoti Gupta, Dharmendra P. Singh, Bhawani S. Joshi, Raja Roy, Anjani K. Mishra, Ram Pratap
Publikováno v:
ARKIVOC, Vol 2010, Iss 9, Pp 1-11 (2010)
Externí odkaz:
https://doaj.org/article/f9bf2af99a8b4e6e82eb4e5771f62e84
Autor:
Ram Pratap, Priti Khemaria, Bhawani S. Joshi, Dharmendra Singh, Raja Roy, Jyoti Gupta, Anjani K. Mishra, Alok Kumar Verma
Publikováno v:
ARKIVOC, Vol 2010, Iss 9, Pp 1-11 (2010)
The bio-transformation of 3-β-hydroxy-5, 16-dien-pregnane-20-one (CDRI 80/574, 1) a novel antagonist of farnesoid X receptor (FXR) on hepatic membranes, with Aspergillus niger produced the oxidation products at C3 and / or C11 (compound 2 and 3) whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b95766759c596a796f5053ab7f2ff2
https://doi.org/10.3998/ark.5550190.0011.901
https://doi.org/10.3998/ark.5550190.0011.901
Autor:
Chunni Lal Khetrapal, Bhawani S. Joshi, Neeraj Sinha, Sudhir Kumar Mandal, Santosh Kumar Bharti, Raja Roy
Publikováno v:
Metabolomics. 4:367-376
A method of choosing the correction factor based on Bloch equation for the quantitative estimation of metabolite from 1H NMR spectra recorded with reduced recycle delay is prescribed. The procedure reduces the experimental time without substantially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c996bc4c441f7b76d4083bd8a35a3bd2
https://doi.org/10.1007/s11306-008-0130-6
https://doi.org/10.1007/s11306-008-0130-6
Autor:
Bhawani S. Joshi, Amit Nag, Harapriya Rath, Tavarekere K. Chandrashekar, Viswanathan Prabhuraja, Debabrata Goswami
Publikováno v:
Organic Letters. 8:2325-2328
[structure: see text] Core-modified aromatic decaphyrins with 42pi conjugated electrons exhibit the highest two-photon absorption cross-section value (sigma(2) = 108,000 GM) known for any organic molecule, suggesting possible device applications in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422586ec79cb6aa9baae877b33d11ff2
https://doi.org/10.1021/ol060622a
https://doi.org/10.1021/ol060622a
Autor:
Raja Roy, Dharam C. Jain, Bhawani S. Joshi, Urszula Rychlewska, R. P. Sharma, Mahesh Pal, Asish K. Bhattacharya
Publikováno v:
Tetrahedron. 59:2871-2876
Absolute stereochemistry of dihydroarteannuin B 5 obtained by the reduction of arteannuin B 3 with Ni2B, NaBH4 or CdCl2–Mg–MeOH–H2O has been established by 2D NMR and single crystal X-ray diffraction studies. Some experiments aimed at the synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::583e27abbff69037458ce42845181896
https://doi.org/10.1016/s0040-4020(03)00330-2
https://doi.org/10.1016/s0040-4020(03)00330-2
Publikováno v:
The Journal of Organic Chemistry. 67:5783-5788
The Baylis−Hillman (BH) reaction of substituted 5-isoxazolecarboxaldehydes with cyclohexenone in the presence of TiCl4 invariably lead to the formation of hemiacetals beside the BH adducts. A similar reaction in the presence of DABCO, DBU, or 3-HQN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a434ff67d5e6e08b7d6b68fac4b64dad
https://doi.org/10.1021/jo020199t
https://doi.org/10.1021/jo020199t
Autor:
Bhawani S. Joshi, Raja Roy, Simi K. Pushpan, Venkataramanarao G. Anand, Alagar Srinivasan, Tavarekere K. Chandrashekar
Publikováno v:
Journal of Porphyrins and Phthalocyanines. :410-422
The detailed 1 H and 13 C NMR analysis of 5,10,19,24-tetramesityl-33,35,36,38,39-pentathiaheptaphyrin (1) and 5,10,19,24-tetraphenyl-35,36-dioxa-33,38,39-trithiaheptaphyrin (2) in the native and protonated state were carried out using two-dimensional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02143ad7311e4aafd16374ef73a4a15d
https://doi.org/10.1142/s1088424602000518
https://doi.org/10.1142/s1088424602000518
Autor:
Ashok Kumar Khanna, Amiya P. Bhaduri, Sanjay Batra, Ramesh Chander, Bhawani S. Joshi, Raja Roy
Publikováno v:
Bioorganic & Medicinal Chemistry. 9:3093-3099
A new series of compounds belonging to N,N'- [bis (1-aryl-6-hydroxy-hex-2-ene-1-one-3-yl)-1,n-alkanediamines (2-5a-f) have been synthesized and evaluated for antioxidant and hypolipidemic activities. Amongst all the synthesized compounds, seven compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2243d571181fac5e6981c2b6627ea232
https://doi.org/10.1016/s0968-0896(01)00185-7
https://doi.org/10.1016/s0968-0896(01)00185-7
Core-Modified Hexaphyrins; Characterization of Two- and Four-Ring Inverted 26 π Aromatic Macrocycles
Autor:
Uwe Schilde, Sundararaman Venkatraman, Bhawani S. Joshi, Mathias O. Senge, C. L. Khetrapal, Harapriya Rath, Venkataramanarao G. Anand, Jeyaraman Sankar, Tavarekere K. Chandrashekar
Publikováno v:
Organic Letters. 5:3531-3533
[reaction: see text] Synthesis and structural characterization of aromatic core-modified 26 pi hexaphyrin analogues are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::990a712807a90615c9023e0225273b97
https://doi.org/10.1021/ol035408q
https://doi.org/10.1021/ol035408q
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81b4c8bcff7351e56b9f568c88de7dcf
https://doi.org/10.1002/chin.200122100
https://doi.org/10.1002/chin.200122100