Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 231,149,139 papers from all fields of science
Search
Sign In
Create Free Account
Mandibular right lateral incisor abutment
Known as:
26a
National Institutes of Health
Create Alert
Alert
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Studies on the total synthesis of lactonamycin: construction of model ABCD ring systems.
D. Henderson
,
Philip N. Collier
,
+4 authors
A. Barrett
Journal of Organic Chemistry
2006
Corpus ID: 36403172
Model studies on the synthesis of the tetracyclic ABCD ring system of lactonamycin (1) are described. The key step involved the…
Expand
Highly Cited
2004
Highly Cited
2004
Die Spermatocytenteilungen der Tipuliden
H. Bauer
,
R. Dietz
,
Christa RÖbbelen
Chromosoma
2004
Corpus ID: 39610631
Summary1.Chromosomal rearrangements in Tipula oleracea have been induced by X-raying mature sperms, and have been studied in…
Expand
2004
2004
An atom-economical approach to conformationally constrained tricyclic nitrogen heterocycles via sequential and tandem Ugi/intramolecular Diels-Alder reaction of pyrrole.
K. Paulvannan
Journal of Organic Chemistry
2004
Corpus ID: 20190334
An efficient approach to rigid tricyclic nitrogen heterocycles via sequential and tandem Ugi/intramolecular Diels-Alder (IMDA…
Expand
2003
2003
Synthesis and properties of Bingel-type methanofullerene-pi-extended-TTF diads and triads.
S. González
,
N. Martín
,
D. Guldi
Journal of Organic Chemistry
2003
Corpus ID: 37536604
Novel C(60)/pi-extended tetrathiafulvalene (exTTF) diads (12a-c) and triads [D(2)A (14a-c) and DA(2) (25, 27a-c)] have been…
Expand
2002
2002
2a-[4-(Tetrahydropyridoindol-2-yl)butyl]tetrahydrobenzindole derivatives: new selective antagonists of the 5-hydroxytryptamine7 receptor.
C. Kikuchi
,
T. Ando
,
+4 authors
M. Koyama
Journal of Medicinal Chemistry
2002
Corpus ID: 42804951
A series of tetrahydrobenzindoles was prepared, and the affinity of these compounds for the 5-hydroxytryptamine7 (5-HT7) receptor…
Expand
Highly Cited
2000
Highly Cited
2000
Stereoselective preparation of enantiomerically pure annulated carbohydrates using ring-closing metathesis
Holt
,
Barker
,
Jenkins
,
Panda
,
Ghosh
Journal of Organic Chemistry
2000
Corpus ID: 9415588
Ring-closing metathesis has been applied to a series of glucose derivatives to produce cyclopentene derivatives 5a and 5b…
Expand
Highly Cited
2000
Highly Cited
2000
Synergistic Formation of Soluble Lectin Clusters by a Templated Multivalent Saccharide Ligand
S. D. Burke
,
Qian Zhao
,
M. Schuster
,
L. Kiessling
2000
Corpus ID: 84915931
Protein-carbohydrate recognition events mediate significant biological processes including fertilization, pathogen-cell adhesion…
Expand
Highly Cited
1999
Highly Cited
1999
Biradicals from Thermolysis of N-[2-(1-Alkynyl)phenyl]-N'-phenylcarbodiimides and Their Subsequent Transformations to 6H-Indolo[2,3-b]quinolines.
C. Shi
,
Quan Zhang
,
Kung K. Wang
Journal of Organic Chemistry
1999
Corpus ID: 25769726
Thermolysis of the carbodiimide 9a in gamma-terpinene at 138 degrees C produced 2-(phenylamino)quinoline (11a, 49%) and the…
Expand
1997
1997
The vitamin D analog, KH1060, is rapidly degraded both in vivo and in vitro via several pathways: principal metabolites generated retain significant biological activity.
F. J. Dilworth
,
G. Williams
,
+5 authors
G. Jones
Endocrinology
1997
Corpus ID: 6343858
Vitamin D analogs are valuable drugs with established and potential uses in hyperproliferative disorders. Lexacalcitol (KH1060…
Expand
1987
1987
Synthesis and calcium channel antagonist activity of dialkyl 4- (dihydropyridinyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinecarboxylates.
L. Dagnino
,
M. C. Li-Kwong-Ken
,
H. Wynn
,
M. Wolowyk
,
C. Triggle
,
E. Knaus
Journal of Medicinal Chemistry
1987
Corpus ID: 24251962
The sodium borohydride reduction of 3,5-disubstituted 1,4-dihydro-2,6-dimethyl-4-(pyridinyl)pyridines 2 and 5 in the presence of…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE