Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Bandi Chennakesava Reddy"'
Publikováno v:
Helvetica Chimica Acta. 96:266-274
A stereoselective total synthesis of multiplolide A (1) and of its diastereoisomer 2 was described from easily accessible starting materials (Schemes 2–4). The synthetic strategy involves a Jacobsen resolution, Sharpless epoxidation, Swern oxidatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::865487f4a7fe58b3d0f99462cc18d0aa
https://doi.org/10.1002/hlca.201200164
https://doi.org/10.1002/hlca.201200164
Autor:
Harshadas M. Meshram, Vikas M. Bangade, Bandi Chennakesava Reddy, Gudimella Santosh Kumar, Pramod B. Thakur
Publikováno v:
International Journal of Organic Chemistry. :159-165
The synthesis of C-substituted and N-substituted pyrrole is described by the reaction of phenacyl bromides, pentane-2, 4-dione and amine in aqueous medium using DABCO as a catalyst. The method is very convenient and applicable for alkyl as well as ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::819473a7f071b04181cde650e7ea98a4
https://doi.org/10.4236/ijoc.2012.22024
https://doi.org/10.4236/ijoc.2012.22024
Autor:
Harshadas M. Meshram, Palakuri Ramesh, Bandi Chennakesava Reddy, Balasubramanian Sridhar, Jhillu S. Yadav
Publikováno v:
Tetrahedron. 67:3150-3155
An efficient vinylogous Mukaiyama aldol reaction (VMAR) of 2-(trimethylsilyloxy)furan with various (N-alkyl)isatins is described in the presence of lanthanum(III) triflates (5 mol %). The reaction proceeds rapidly and affords the corresponding 3-hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7500a13820bcc24305a17349c11f58d3
https://doi.org/10.1016/j.tet.2011.02.033
https://doi.org/10.1016/j.tet.2011.02.033
Publikováno v:
Helvetica Chimica Acta. 92:1002-1006
An efficient method for the Friedel–Crafts alkylation of 1H-indole with nitro alkenes in the presence of zinc acetate is described. The procedure is applicable to a variety of nitro alkenes and substituted indoles, and the yields are very high.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eae056b1c053a0f7149e7de3110a97ec
https://doi.org/10.1002/hlca.200800410
https://doi.org/10.1002/hlca.200800410
Autor:
Palakuri Ramesh, N. Nageswara Rao, Bandi Chennakesava Reddy, Harshadas M. Meshram, Pramod B. Thakur
Publikováno v:
ChemInform. 45
A highly efficient and convenient synthesis of bis(indolyl)methanes (III) (10 examples) via boric acid promoted reaction of indoles with various aromatic and heteroaromatic aldehydes in an environmentally benign medium is developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::495fb738b2326c47e24c7170b89fc22d
https://doi.org/10.1002/chin.201406137
https://doi.org/10.1002/chin.201406137
Autor:
Palakuri Ramesh, Jhillu S. Yadav, Balasubramanian Sridhar, Bandi Chennakesava Reddy, Harshadas M. Meshram
Publikováno v:
ChemInform. 42
Title reaction provides access towards 3-hydroxy-3-(dihydrofuranyl)indoles in good yields and moderate to good diastereoselectivities (up to 90% d.e.).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a45b38ed7f1def161cc478e7c7c88783
https://doi.org/10.1002/chin.201134113
https://doi.org/10.1002/chin.201134113
Publikováno v:
ChemInform. 40
An efficient method for the Friedel–Crafts alkylation of 1H-indole with nitro alkenes in the presence of zinc acetate is described. The procedure is applicable to a variety of nitro alkenes and substituted indoles, and the yields are very high.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7d3bac5323ec4043a0252c3440e6ae4
https://doi.org/10.1002/chin.200939109
https://doi.org/10.1002/chin.200939109
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