Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Kusum L. Chandra"'
Publikováno v:
ARKIVOC, Vol 2002, Iss 7, Pp 34-45 (2002)
Externí odkaz:
https://doaj.org/article/3d14b9acf1064dfdb02da21cd1410d8d
Publikováno v:
Organic Letters. 13:3718-3721
An efficient three-step synthesis of 2-halo-3-aryl-4(3H)-quinazoliniminium halides from commercially available materials is described. Upon reaction with hydrogen halides, generated in situ from a Lewis acid (MX) and trace water, a variety of easily
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::debafff2f80b81c5c717f5bcd9009742
https://doi.org/10.1021/ol201372n
https://doi.org/10.1021/ol201372n
Autor:
Jean-Pierre Perchellet, Kusum L. Chandra, Andrew M. Waters, Aditya S. Gundugola, Sundeep Rayat, Elisabeth M. Perchellet
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:3920-3924
A series of 1,4-diaryl tetrazol-5-ones were synthesized by copper mediated N-arylation of 1-phenyl-1 H -tetrazol-5(4 H )-one with aryl boronic acids, o -R 1 C 6 H 4 B(OH) 2 where R 1 = H, OMe, Cl, CF 3 , Br, C CH. The 1,4-diaryl tetrazol-5-ones subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17c015555c90aa1fcb6402673511f292
https://doi.org/10.1016/j.bmcl.2010.05.012
https://doi.org/10.1016/j.bmcl.2010.05.012
Publikováno v:
The Journal of Physical Chemistry C. 112:20510-20517
This work addresses a significant challenge in engineered molecular systems regarding both understanding and controlling the stability of molecule/nanoparticle nanostructures under ambient exposure. Results deal specifically with molecular electronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8db7755811af4ee87be081917c539017
https://doi.org/10.1021/jp8066298
https://doi.org/10.1021/jp8066298
Publikováno v:
Tetrahedron. 63:7120-7132
Several methodologies for the selective deprotection acetylenes have been reported previously. However, as is shown here, they are often not reliable or convenient. Here, an approach is reported that is efficient and general. Use of this approach to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5736db8f61bf8dcf0e5af1b947d601eb
https://doi.org/10.1016/j.tet.2007.05.006
https://doi.org/10.1016/j.tet.2007.05.006
Publikováno v:
ARKIVOC, Vol 2002, Iss 7, Pp 34-45 (2002)
A general approach towards synthesis of 5-hydroxyalkylbutan-4-olides from D-mannitol has been described. The approach has been used successfully for total synthesis of (-)-muricatacin, an anti-tumour natural product. Other related natural and unnatur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e54b9770aa41640e1aa1b0d5f039f137
https://doi.org/10.3998/ark.5550190.0003.705
https://doi.org/10.3998/ark.5550190.0003.705
Publikováno v:
The Journal of Organic Chemistry. 67:4630-4633
Total synthesis of (-)-lentiginosine was achieved from D-mannitol using highly stereoselective reactions. Similarly, (+)-lentiginosine was synthesized from L-tartaric acid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::926a862c3a3dc33b41aa74f511d4edef
https://doi.org/10.1021/jo025677e
https://doi.org/10.1021/jo025677e
Publikováno v:
Tetrahedron. 57:241-247
Aromatic electrophilic substitution reactions such as alkylation, acylation, benzoylation, and sulfonylation were studied in the presence of a catalytic amount of Cu(OTf) 2 and Sn(OTf) 2 . Cu(OTf) 2 was very efficient for alkylation, acylation, and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::480b9a23d19a632135b868d124c14f64
https://doi.org/10.1016/s0040-4020(00)01005-x
https://doi.org/10.1016/s0040-4020(00)01005-x
Publikováno v:
Journal of Chemical Research. 2002:221-223
A variety of epoxides were converted into β-chloroacetates and benzoates by using TMSCl and the corresponding acid anhydride in the presence of a catalytic amount of Cu(OTf)2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c963f0a5fc641ce44362f3897388cda1
https://doi.org/10.3184/030823402103171924
https://doi.org/10.3184/030823402103171924
Publikováno v:
Tetrahedron Letters. 43:2773-2775
A general approach towards the synthesis of 5-hydroxyalkylbutan-4-olides from D-mannitol has been described. The approach has successfully been used for the total synthesis of (-)-muricatacin, an anti-tumor natural product.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6462d0aa001b373c990478852484478
https://doi.org/10.1016/s0040-4039(02)00375-1
https://doi.org/10.1016/s0040-4039(02)00375-1