Dear prof. Ackermann,
I am very keen to do my PhD under your skilled supervision at the University of Gottingen, and I have strong enthusiasm to become one of your research group members, and I feel that I have the necessary qualifications and abilities to join your group.
Your publications in the field of organic synthesis, with a specific focus on C-H, and C-C activation, were so exciting to me. I have studied some of your articles and was very impressed by the way you utilized various methods and alternative catalysts for C-C, and C-H alkylation. In one of your articles, you mentioned the use of manganese, as a less toxic catalyst, for C-H activation in indole toward peptide synthesizing. This method had functional group tolerance, and also was in good to excellent yield. In another report, you used rhodium as a catalyst for electro-oxidative C-C alkylation, and introduced the first electro-chemical C-C activation by using electricity, via a greener way due to the fact that it was oxidant-free. As a result, studying your research works motivated me to try joining your research lab.
I was extremely interested in synthesis, especially synthesizing bioactive compounds. Therefore, I chose medicinal chemistry as my field of study. Throughout bachelor, I was the top student in organic chemistry courses. To pass my master’s internship course, I worked under supervision of Dr. Majid Hamzeloo in chemistry physics lab, University of Tehran. The main topic of my research was the study of physio-chemical properties of several drugs to increase their absorption time. This limited research gave me the opportunity to push my knowledge boundaries further.
My greater curiosity and interest in chemistry pushed me to pursue my education and led me to several achievements in my field of study. During my master, I had 5 lectures in the field of medicinal chemistry, biochemistry, and synthesis. My lectures in biochemistry were entitled “DNA Polymerase II” and “Antiviral Nucleoside analogues” and the other in the field of medicinal chemistry was about “Non-Alcoholic Fatty Liver disease “and introducing some common medicines for this prevalent disease. My master’s thesis was entitled “Synthesis of 2H-Azirines and their usage in designing of new reactions”. I tried several reactions with this highly potent ring, and I did never give up until getting an acceptable result. I synthesized 23 derivatives of my final product in a limited time. As you studied my research experience, I was also able to get an excellent response by using a totally different electrophile (Iodine), and I synthesized 5 derivatives of this target product within just one week. During my master thesis, I tried to focus on improving my skills in organic synthesis, and Joining Balalaie’s research group gave me the opportunity to gain communicative and teamwork skills as well as Specialized skills in synthesis, purification, and characterization of organic compounds.
Finally, I hope you accept me as one of your group’s member to be able to play a crucial role in your research activities. I am so interested in working in an academic environment after finishing my PhD, and it is my honor to learn from you and accompany you in this area, and I believe that I am able to meet the challenges which I have prepared myself as well as I could.
Sincerely,
Reyhaneh Hosseinijei
Dear prof.  
Ackermann
,
I am  
very
 keen to do my PhD under your skilled supervision at the University of  
Gottingen
, and I have strong enthusiasm to become one of your  
research
  group
 members, and I feel that I have the necessary qualifications and abilities to  
join
 your group.
Your publications in the  
field
 of  
organic
  synthesis
, with a specific focus on C-H, and C-C activation, were  
so
 exciting to me. I have studied  
some
 of your articles and was  
very
 impressed by the way you utilized various methods and alternative catalysts for C-C, and C-H  
alkylation
. In one of your articles, you mentioned the  
use
 of manganese, as a less toxic catalyst, for C-H activation in  
indole
 toward peptide synthesizing. This method had functional  
group
 tolerance, and  
also
 was in  
good
 to excellent yield. In another report, you  
used
 rhodium as a catalyst for  
electro-oxidative
 C-C  
alkylation
, and introduced the  
first
  electro-chemical
 C-C activation by using electricity, via a greener way due to the fact that it was oxidant-free.  
As a result
, studying your  
research
 works motivated me to try joining your  
research
 lab.
I was  
extremely
 interested in  
synthesis
,  
especially
 synthesizing bioactive compounds.  
Therefore
, I chose medicinal  
chemistry
 as my  
field
 of study. Throughout bachelor, I was the top student in  
organic
  chemistry
 courses. To pass my  
master’s
 internship course, I worked under supervision of Dr. Majid  
Hamzeloo
 in  
chemistry
 physics lab, University of Tehran. The main topic of my  
research
 was the study of physio-chemical properties of several drugs to increase their absorption time. This limited  
research
 gave me the opportunity to push my knowledge boundaries  
further
.
My greater curiosity and interest in  
chemistry
 pushed me to pursue my education and led me to several achievements in my  
field
 of study. During my  
master
, I had 5 lectures in the  
field
 of medicinal  
chemistry
, biochemistry, and  
synthesis
. My lectures in biochemistry  
were entitled
 “DNA Polymerase II” and “Antiviral Nucleoside analogues” and the other in the  
field
 of medicinal  
chemistry
 was about “Non-Alcoholic Fatty Liver disease “and introducing  
some
 common medicines for this prevalent disease. My  
master’s
 thesis  
was entitled
  “Synthesis
 of 2H-Azirines and their usage in designing of new reactions”. I tried several reactions with this  
highly
 potent ring, and I did never give up until getting an acceptable result. I synthesized 23 derivatives of my final product in a limited time. As you studied my  
research
 experience, I was  
also
 able to  
get
 an excellent response by using a  
totally
  different
  electrophile
 (Iodine), and I synthesized 5 derivatives of this target product within  
just
 one week. During my  
master
 thesis, I tried to focus on improving my  
skills
 in  
organic
  synthesis
, and Joining  
Balalaie
’s  
research
  group
 gave me the opportunity to gain communicative and teamwork  
skills
  as well
 as Specialized  
skills
 in  
synthesis
, purification, and characterization of  
organic
 compounds. 
Finally
, I hope you accept me as one of your  
group’s
 member to be able to play a crucial role in your  
research
 activities. I am  
so
 interested in working in an academic environment after finishing my PhD, and it is my honor to learn from you and accompany you in this area, and I believe that I am able to  
meet
 the challenges which I have prepared myself  
as well
 as I could. 
Sincerely
, 
Reyhaneh
  Hosseinijei