Qin Lab
@QinLab
Followers
546
Following
137
Media
2
Statuses
11
Interested in PhD in Biochemistry or Organic Chemistry? Register for UTSouthwestern Virtual Grad Student Recruitment Symposium for Underrepresented Minority Students on Nov 20 https://t.co/Tkqz7RrBFF
@utsw_bc_diverse @TAAASatUTSW @SACNASatUTSW @UTSWGradSchool @ADiaz_PhD @Nstree37
0
73
71
The final version of this study (collaboration with @rohanmerchant1 #MerckChemistry) has appeared in @NatureChemistry
https://t.co/SqtWx18SfB Thanks to Dr. Brocklehurst and @EdAndersonGroup for the highlights
We are excited to share our latest collaboration with @Merckchemistry @rohanmerchant1 to develop a new (non strain-release) approach to access bicyclo[1.1.1]pentanes (BCPs) with C1, C2 and/or C3 substitutions. https://t.co/nY2udUZQBr
1
16
123
Check out our latest synthesis of the heavily rearranged steroid natural products pinnigorgiols using a semisynthetic approach, out now in @J_A_C_S : https://t.co/bj2u5SZ8GO
pubs.acs.org
Pinnigorgiols B and E are 9,11-secosteroids with a unique tricyclic γ-diketone framework. Herein, we report the first synthesis of these natural products from inexpensive, commercially available...
5
18
118
Our latest work on the biomimetic synthesis and structural revision of sarocladione, out now in @angew_chem as a VIP paper, is enabled by the development of a novel ruthenium-catalyzed endoperoxide fragmentation: https://t.co/65GlKbXKGr
5
19
135
After having thought about the dehydoxylative cross-coupling for years (since I was a postdoc in Baran Lab @BaranLabReads), we finally figured out an expedient method @J_A_C_S:
pubs.acs.org
As alcohols are ubiquitous throughout chemical science, this functional group represents a highly attractive starting material for forging new C–C bonds. Here, we demonstrate that the combination of...
4
26
185
Today in @ChemRxiv ( https://t.co/6obdN8fJ89) a collaborative study on a combinatorial approach to oxidizing sp3-C–H bonds. N-ammonium ylide-based oxidants: Developed based on first principles, guided by computation, and activated electrochemically. Modular, selective, simple.
1
34
216
We are excited to share our latest collaboration with @Merckchemistry @rohanmerchant1 to develop a new (non strain-release) approach to access bicyclo[1.1.1]pentanes (BCPs) with C1, C2 and/or C3 substitutions. https://t.co/nY2udUZQBr
5
27
205
We are pleased to share our recent collaborative effort with Rohan and Jonathan from Merck, to access hindered alkyl boron compounds. @rohanmerchant1
https://t.co/kUkk6GStRN
4
23
112