/ Home
/ SUBMISSION

/ The BJOC
/ Diamond Open Access
/ Journal Statistics
/ Editorial Board
/ Community
/ Call for papers

/ Latest Articles
/ Most accessed
/ Thematic issues
/ Volumes
/ Authors

/ Alerts

/ TWITTER
/ LINKEDIN
/ Mastodon
/ RSS FEED

Empty search

Article Type

Publication Date Range

Search Tips

This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.

Search Examples

aromatic	the word “aromatic”
aromatic aldehyde	the word “aromatic” OR “aldehyde”
+aromatic +aldehyde	both words “aromatic” AND “aldehyde”
+aromatic -aldehyde	the word “aromatic” but NOT “aldehyde”
“aromatic aldehyde”	the exact phrase “aromatic aldehyde”
benz*	words which begin with “benz”, such as “benzene” or “benzyl”
benz*yl	words that begin with “benz” and end with “yl”, such as “benzyl” or “benzoyl”
benzyl~	words that are close to the word “benzyl”, such as “benzoyl” (i.e., fuzzy search)

BROWSE
Latest Articles
Most accessed
thematic issues
volumes
authors

BROWSE

Latest Articles Most Accessed Thematic Issues Volumes Authors

Author

1 article(s) from Rudlof, Jens

Asymmetric synthesis of propargylamines as amino acid surrogates in peptidomimetics

Matthias Wünsch,
David Schröder,
Tanja Fröhr,
Lisa Teichmann,
Sebastian Hedwig,
Nils Janson,
Clara Belu,
Jasmin Simon,
Shari Heidemeyer,
Philipp Holtkamp,
Jens Rudlof,
Lennard Klemme,
Alessa Hinzmann,
Beate Neumann,
Hans-Georg Stammler and
Norbert Sewald

Beilstein J. Org. Chem. 2017, 13, 2428–2441, doi:10.3762/bjoc.13.240

PDF

Graphical Abstract

Figure 1: Concept of carboxylic acid or amide bond replacement on the basis of an alkyne moiety.

Jump to Figure 1

Figure 2: Selection of reactions based on propargylamines as precursors. a) Intramolecular Pauson–Khand react...

Jump to Figure 2

Figure 3: Two different approaches for the stereoselective de novo synthesis of propargylamines using Ellman’...

Jump to Figure 3

Figure 4: Synthesis of propargylamines 4a and 4b by introducing the side chain as nucleophile. (a) HC≡CCH₂OH,...

Jump to Figure 4

Figure 5: Reaction of N-sulfinylimine 5h with (trimethylsilyl)ethynyllithium. (a) GP-3 or GP-4. (b) Aqueous w...

Jump to Figure 5

Figure 6: Side reactions observed in the course of the conversion of highly electrophilic sulfinylimines 5. (...

Jump to Figure 6

Figure 7: a) Possible transition states TI and TII for the transfer of the methyl moiety from AlMe₃ to the im...

Jump to Figure 7

Figure 8: Base-induced rearrangement of propargylamines bearing electron-withdrawing substituents.

Jump to Figure 8

Figure 9: Base-catalyzed rearrangement of propargylamines 11 to α,β-unsaturated imines 12. A) Reaction scheme...

Jump to Figure 9

Album

Supp Info

Full Research Paper

Published 15 Nov 2017

Full text

Other Beilstein-Institut Open Science Activities

/ Help / Support & Contact / Alerts / Privacy Policy / Terms & Conditions / Impressum