Zobrazeno 1 - 10
of 18
pro vyhledávání: '"J. Satyanarayana Reddy"'
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 11, Pp o2961-o2961 (2011)
In the crystal structure of the title compound, C15H9NO4, weak C—H...O interactions generate rings with R22(8) motifs. The supramolecular aggregation is completed by the presence of C—H...O and van der Waals interactions.
Externí odkaz:
https://doaj.org/article/89b6761be36e47499e739b65ae7d55a1
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 6, Pp o1330-o1330 (2011)
In the title compound, C16H12O4, the 1-benzofuranone unit is in a planar conformation [C—C—C—C = 179.69 (12)°]. The conformation around the C=C double bond [1.3370 (17) Å] is Z. In the crystal, the molecules are stabilized by O—H...O (runni
Externí odkaz:
https://doaj.org/article/5cf0e9fd59c04fc090985914e4fa5187
Publikováno v:
European Journal of Organic Chemistry. 2015:840-846
A simple and efficient method for the prepn. of β-hydroxyacylsilanes has been developed through a TiCl4-mediated aldol reaction of acylsilanes with aldehydes. Acylsilane EtCOSiMe2Ph reacted with PhCHO giving 80:20 diastereomeric syn-anti mixt. of Ph
Autor:
K. Anand Solomon, J. Satyanarayana Reddy, N. Ravikumar, Gopikrishna Gaddamanugu, K.N. Naresh, S. S. Rajan
Publikováno v:
Journal of Molecular Structure. 1039:137-143
α-Mangostin is a naturally occurring oxygenated xanthonoid isolated from the mangosteen tree (Garcinia mangostana). We report the molecular salts of α-mangostin with the active pharmaceutical ingredients (APIs) metformin (anti-diabetic) and piperaz
Publikováno v:
Journal of Chemical Sciences. 123:673-679
A convenient, catalyst-free protocol for the quantitative synthesis of fused chromeno[4,3-b]quinolin-6-ones has been developed by simple one-pot reaction of substituted anilines with 4-chloro-3-formylcoumarin using ultrasound irradiation. The protoco
Autor:
K. Anil Kumar, K. Anand Solomon, Saraswatula Viswanadha Ganesh, Ashwini Nangia, N. Rajesh Goud, Ravikumar Nagalapalli, J. Satyanarayana Reddy, Rambabu Dandela
Publikováno v:
Journal of Pharmaceutical Sciences. 100:3160-3176
The crystallization of fluoroquinolone antibiotics norfloxacin and ciprofloxacin with carboxylic acids gave six new salts that were characterized by infrared spectroscopy, differential scanning calorimetry, X-ray powder diffraction, and single crysta
Autor:
N. Thrimurtulu, Jhillu S. Yadav, B. V. Subba Reddy, Md. Ataur Rahman, J. Satyanarayana Reddy, A. R. Prasad
Publikováno v:
Synthesis. 2010:3657-3662
A practical stereoselective total synthesis of (3R,5R)-5-hydroxy-de-O-methyllasiodiplodin has been accomplished via Prins cyclization. It exhibits potato microtuber inducing activity. The synthetic sequence involves Prins cyclization, reductive openi
Publikováno v:
ChemInform. 46
Synthetically important β-hydroxyacylsilanes are available with good to excellent diastereoselectivity under mild conditions.
Autor:
J. Satyanarayana Reddy, Jhillu S. Yadav, Akondi Srirama Murthy, Saibal Das, Gangireddy PavanKumar Reddy, Thierry Roisnel, René Grée, Srivari Chandrasekhar
Publikováno v:
ChemInform. 45
Three complementary strategies have been explored to obtain stereodefined 1,3 diols starting from easily accessible syn β-hydroxy acylsilanes: fluoride induced migrations of substituents on silicon, a Grignard addition followed by protodesilylation
Autor:
Saibal Das, Jhillu S. Yadav, Akondi Srirama Murthy, Gangireddy PavanKumar Reddy, René Grée, Thierry Roisnel, J. Satyanarayana Reddy, Srivari Chandrasekhar
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2014, 55 (2), pp.365-368. ⟨10.1016/j.tetlet.2013.11.034⟩
Tetrahedron Letters, 2014, 55 (2), pp.365-368. ⟨10.1016/j.tetlet.2013.11.034⟩
Tetrahedron Letters, Elsevier, 2014, 55 (2), pp.365-368. ⟨10.1016/j.tetlet.2013.11.034⟩
Tetrahedron Letters, 2014, 55 (2), pp.365-368. ⟨10.1016/j.tetlet.2013.11.034⟩
Three complementary strategies have been explored to obtain stereodefined 1,3 diols starting from easily accessible syn β-hydroxy acylsilanes: fluoride induced migrations of substituents on silicon, a Grignard addition followed by protodesilylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1673bf1403e5aac7e1dea524a0b7f74d
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01114434
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01114434