Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Srinu Tothadi"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 80, Iss 3, Pp 310-313 (2024)
An attempt to explore the reactivity of the nitro group in the presence of gold catalysis in comparison to the azide group yielded intriguing results. Surprisingly, only the nitro group exhibited reactivity, ultimately giving rise to the formation of
Externí odkaz:
https://doaj.org/article/cd694f5a14c649f8a9c28d9b0c3e2c36
Autor:
Jayasubba Reddy Yarava, Lokeswara Rao Potnuru, Bholanath Pahari, Srinu Tothadi, K.V. Ramanathan
Publikováno v:
Journal of Magnetic Resonance Open, Vol 10, Iss , Pp 100056- (2022)
Supramolecular synthons are the smallest structural units that contain the information inherent in building large molecular assemblies. Here, we apply solid-state NMR methods for the identification of the synthon in a cocrystal of Azelaic acid [(CH2)
Externí odkaz:
https://doaj.org/article/b419b2849ac841688ff541ebef87a593
Publikováno v:
Inorganics, Vol 10, Iss 7, p 97 (2022)
In this paper, we have used a saturated five-membered N-Heterocyclic carbene (5SIDipp = 1,3-bis-(2,6-diisopropylphenyl)imidazolin-2-ylidine) for the synthesis of SNHC-haloboranes adducts and their further nucleophilic substitutions to put unusual fun
Externí odkaz:
https://doaj.org/article/9246e163177d4b96b793119ad0a219a9
Autor:
Sunil K. Rai, Srinu Tothadi, Mihails Arhangelskis, Christy P. George, Rajesh G. Gonnade, Ashwini K. Nangia
Publikováno v:
CrystEngComm. 25:2712-2716
Form II of hydroxyurea (HU) has been crystallized in the presence of urea in methanol solvent. The isoenergetic novel form II is isolated 150 years after its first synthesis (form I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce41f0b1a5c877a85c319d62cb8a158d
https://doi.org/10.1039/d3ce00163f
https://doi.org/10.1039/d3ce00163f
Publikováno v:
IUCrJ, Vol 5, Iss 6, Pp 816-822 (2018)
The single-crystal X-ray structure of a 6-component organic-salt alloy (hexanary) of naftopidil (1) (an active pharmaceutical ingredient) with benzoic acid (2) and four different hydroxy-substituted benzoic acids, i.e. salicylic acid (3), 2,3-dihydro
Externí odkaz:
https://doaj.org/article/3bd1b672b6e84b24a28f5c618af17d6f
Publikováno v:
Organometallics. 41:3706-3717
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db58be8514bde83d76f77add99ee108d
https://doi.org/10.1021/acs.organomet.2c00480
https://doi.org/10.1021/acs.organomet.2c00480
Autor:
Ashwini Kaushik, Karan Marvaniya, Yamini Kulkarni, Dhruv Bhatt, Jahanvi Bhatt, Manoj Mane, E. Suresh, Srinu Tothadi, Ketan Patel, Shilpi Kushwaha
Publikováno v:
Chem. 8:2749-2765
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcc590cf497f0b72836cae9a804fcf22
https://doi.org/10.1016/j.chempr.2022.07.009
https://doi.org/10.1016/j.chempr.2022.07.009
Publikováno v:
European Journal of Inorganic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83fb6612fd5757de149673c60b68b9c1
https://doi.org/10.1002/ejic.202300167
https://doi.org/10.1002/ejic.202300167
Substitution at sp3 boron of a six-membered NHC·BH3: convenient access to a dihydroxyborenium cation
Publikováno v:
Chemical Communications. 58:3783-3786
6-SIDipp·BH3 (1) was reacted with I2 to give corresponding iodoboranes (2 & 3), which underwent nucleophilic substitution reactions to furnish OTf and ONO2 substituted boranes (4–7). Treatment of Br2/H2O with 1 led to a dihydroxyborenium cation (8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cef7362639057755518487fbff16c16
https://doi.org/10.1039/d1cc06816d
https://doi.org/10.1039/d1cc06816d
Publikováno v:
Dalton Transactions. 51:14452-14457
While 6-SIDipp cleaves the B–H bond of pinacolborane (HBpin) to afford the desired 1,1-oxidative-addition product (7), it undergoes ring expansion with 9-borabicyclo[3.3.1]nonane (9-BBN), leading to a seven-membered ring (6b).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83c9debea842ba35d3d53266565c61c8
https://doi.org/10.1039/d2dt01707e
https://doi.org/10.1039/d2dt01707e