Skip to content
RDL
Network
Ecosystem
Switch app
TR
About
FAQ
Sign in
Get started
ChemInform Abstract: Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture. — Rebecca Johnson (2015) | RDL Network
Back
Cite
Save
Save for later
Share
Home
Publications
ChemInform Abstract: Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.
Shared by
Jay D Keasling
University of California, Berkeley
ChemInform Abstract: Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.
Article
2015
en
Authors
+2 more
RJ
Rebecca Johnson
TR
Tristan de Rond
VL
Vincent N. G. Lindsay
Abstract
1 min read
Abstract Both enantiomers of cycloprodigiosin are synthesized.
Discussion
(0)
Sign in
to like and join the discussion.
No comments yet. Be the first to comment.
Related publications
Article
2015
Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture
Rebecca Johnson
,
Tristan de Rond
,
Vincent N. G. Lindsay
,
Jay D Keasling
,
Richmond Sarpong
Article
2000
The Cyclohexene Ring System as a Furanose Mimic: Synthesis and Antiviral Activity of Both Enantiomers of Cyclohexenylguanine
Jing Wang
,
Matheus Froeyen
,
Chris Hendrix
,
Graciela Andreï
,
Robert Snoeck
,
De Clercq Erik
,
Piet Herdewijn
Article
2013
ChemInform Abstract: Synthesis of Some Novel Thiosemicarbazone Derivatives Having Anticancer, anti‐HIV as well as Antibacterial Activity.
Hitesh D. Patel
,
Saavani Malove Divatia
,
De Clercq Erik
Article
2013
ChemInform Abstract: Synthesis and Evaluation of Novel 4‐Substituted Styryl Quinazolines as Potential Antimicrobial Agents.
Rahul P. Modh
,
Amit C. Patel
,
Dharmesh H. Mahajan
,
Christophe Pannecouque
,
De Clercq Erik
,
Kishor H. Chikhalia
Article
2011
ChemInform Abstract: Synthesis and Biological Evaluation of New 3‐Trifluoromethylpyrazolesulfonyl‐urea and Thiourea Derivatives as Antidiabetic and Antimicrobial Agents.
Hassan M. Faidallah
,
Khalid Ali Khan
,
Abdullah Mohamed Asiri
Discussion(0)
No comments yet. Be the first to comment.