Stereoselective alkylations of a bicyclic lactam derived from pyroglutamic acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Pseudo-A(1,3) Strain as a Key Conformational Control Element in the Design of Poly-l-proline Type II Peptide Mimics
2. Conformational stability of proline oligomers
3. Conversion of L-pyroglutamic acid to 4-alkyl-substituted L-prolines. The synthesis of trans-4-cyclohexyl-L-proline
4. Synthesis of (2S,4S) 2-carboxy-4-pyrrolidine acetic acid, a conformationally constrained 2-amino adipic acid analogue
5. Stereoselective methylations of bicyclic lactams derived from pyroglutamic acid
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3. Lithium Enolates Derived from Pyroglutaminol: Mechanism and Stereoselectivity of an Azaaldol Addition;Journal of the American Chemical Society;2016-08-08
4. Lithium Enolates Derived from Pyroglutaminol: Aggregation, Solvation, and Atropisomerism;The Journal of Organic Chemistry;2016-04-25
5. Uncatalysed diaryldiazo cyclopropanations on bicyclic lactams: access to annulated prolines;Organic & Biomolecular Chemistry;2015
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