Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ajay K. Mandal"'
Autor:
Banwari Lal, Anil Aginihotri, Priyangshu M. Sarma, H.S. Jayasinghearachchi, Sneha Singh, Ajay K. Mandal
Publikováno v:
International Journal of Hydrogen Energy. 34:7197-7207
Present study investigated fermentative hydrogen production of two novel isolates of Enterobacter aerogenes HGN-2 and HT 34 isolated from oil water mixtures. The two isolates were identified as novel strains of E. aerogenes based on 16S rRNA gene. Th
Autor:
Ian N. Fleming, Ajay K. Mandal
Publikováno v:
ChemInform. 30
The hemiacetals 15 and 18 gave cyclopropanols 17 and 20 when treated with NaH in DMSO, showing that the silyl group has enhanced electrofugal powers because of the participation of the oxyanion.
Autor:
Ian Fleming, Ajay K. Mandal
Publikováno v:
ChemInform. 33
Autor:
Sarah C. Archibald, David J. Barden, Jerome F. Y. Bazin, Ian Fleming, Colin F. Foster, Ajay K. Mandal, Amit K. Mandal, David Parker, Ken Takaki, Anne C. Ware, et al. et al.
Publikováno v:
ChemInform. 35
Autor:
Sarah C, Archibald, David J, Barden, Jérôme F Y, Bazin, Ian, Fleming, Colin F, Foster, Ajay K, Mandal, Amit K, Mandal, David, Parker, Ken, Takaki, Anne C, Ware, Anne R B, Williams, Anna B, Zwicky
Publikováno v:
Organicbiomolecular chemistry. 2(7)
Several approaches to the synthesis of ebelactone A 2 are described, culminating in the synthesis of the benzenesulfonate of 2-epi-ebelactone A 161. All the approaches were based on three fragments A, B and C, originally defined in general terms in,
Autor:
Ian N. Fleming, Ajay K. Mandal
Publikováno v:
Chemical Communications. :923-924
The hemiacetals 15 and 18 gave cyclopropanols 17 and 20 when treated with NaH in DMSO, showing that the silyl group has enhanced electrofugal powers because of the participation of the oxyanion.
Autor:
David J. Barden, Colin Foster, Ken Takaki, Ajay K. Mandal, Sarah C. Archibald, Anna B Zwicky, Ian Fleming, Anne C. Ware, David Parker, Jerome F. Y. Bazin, Amit K. Mandal, Anne R B Williams
Publikováno v:
Organic & Biomolecular Chemistry. 2:1051
Several approaches to the synthesis of ebelactone A 2 are described, culminating in the synthesis of the benzenesulfonate of 2-epi-ebelactone A 161. All the approaches were based on three fragments A, B and C, originally defined in general terms in,