Total Synthesis of (±)‐Phomoidride D

…, IM McDonald, M Inoue, N Taniguchi… - Angewandte Chemie …, 2018 - Wiley Online Library
Described herein is a synthetic strategy for the total synthesis of (±)‐phomoidride D. This
highly efficient and stereoselective approach provides rapid assembly of the carbocyclic core …

Synthesis of polycyclic cyclobutane derivatives by tandem intramolecular Michael-aldol reaction under two complementary conditions: TBDMSOTf-Et3N and TMSI …

M Ihara, T Taniguchi, K Makita, M Takano… - Journal of the …, 1993 - ACS Publications
The treatment of a,| 3-unsaturated esters having a ketone function at an appropriate position
with either TBDMSOTf in the presence of Et3N or TMSI in the presence of (TMS) 2NH …

Brain-derived neurotrophic factor prevents low-frequency inputs from inducing long-term depression in the developing visual cortex

S Kinoshita, H Yasuda, N Taniguchi… - Journal of …, 1999 - Soc Neuroscience
Brain-derived neurotrophic factor (BDNF) is reported to enhance synaptic transmission and
to play a role in long-term potentiation in hippocampus and neocortex. If so, a shortage or …

Enantioselective construction of a quaternary asymmetric carbon center: a versatile synthesis of. alpha.-alkyl. alpha.-amino acids

…, M Takahashi, H Niitsuma, N Taniguchi… - The Journal of …, 1989 - ACS Publications
The enantioselective construction of a qua-ternary asymmetric carbon center was developed
through reaction of the dianions derived from the chiral half esters of monosubstituted …

Highly Potent and Orally Active Non-Peptide Arginine Vasopressin Antagonists for Both V1A and V2 Receptors: Synthesis and Pharmacological Properties of 4'-[(4, 4 …

Y Shimada, N Taniguchi, A Matsuhisa… - Chemical and …, 2000 - jstage.jst.go.jp
A series of compounds structually related to 4'-[(4, 4-difluoro-5-methylidene-2, 3, 4, 5-tetrahydro-1H-1-benzoazepin-1-yl)
carbonyl]-2-phenylbenzanilide were synthesized and evaluated …

Nonpeptide arginine vasopressin antagonists for both V1a and V2 receptors: Synthesis and pharmacological properties of 2-phenyl-4'-(2, 3, 4, 5-tetrahydro-1H-1, 5 …

…, H Koshio, K Sakamoto, N Taniguchi… - Chemical and …, 1998 - jstage.jst.go.jp
A series of compounds structurally related to 2-phenyl-4’-(2, 3, 4, 5—tetrahydro-lH-l, 5-benzodiazepine—l-carbonyl)
benzanilide was synthesized and demonstrated to have arginine …

Novel construction of polycyclic systems fused to cyclobutane by tandem intramolecular Michael-aldol reaction

…, M Takano, K Makita, N Taniguchi… - Journal of the …, 1992 - ACS Publications
Solutions of 4 are stable for weeks when stored at-20 C, but the UV-vis absorption features [Xmal
(e): 356 (1870), 490 (940) nm] at room temperature bleached upon brief application of …

(+)-(2R,5S)-4-[4-Cyano-3-(trifluoromethyl)phenyl]-2,5-dimethyl-N-[6-(trifluoromethyl)pyridin-3- yl]piperazine-1-carboxamide (YM580) as an Orally Potent and …

I Kinoyama, N Taniguchi, A Toyoshima… - Journal of medicinal …, 2006 - ACS Publications
A novel series of trans-N-aryl-2,5-dimethylpiperazine-1-carboxamide derivatives was
synthesized and their androgen receptor (AR) antagonist activities and in vivo antiandrogenic …

Asymmetric total synthesis of tacamonine (pseudovincamone I) via radical cyclization

M Ihara, F Setsu, M Shohda, N Taniguchi… - The Journal of …, 1994 - ACS Publications
The radical cyclizations of (±)-f£)-3-((2-(bromomethyl) butoxy) carbonyl) prop-2-enoates 11
and 12 and (±)-ethyl (£)-3-{/V-[2-(bromomethyl) butyl]-/V-[2-(3-indolyl) ethyl] carbamoyl} prop-…

Nonpeptide arginine vasopressin antagonists for both V1A and V2 Receptors: Synthesis and pharmacological properties of 4'-(1, 4, 5, 6-tetrahydroimidazo [4, 5-d][1] …

A Matsuhisa, N Taniguchi, H Koshio… - Chemical and …, 2000 - jstage.jst.go.jp
Arginine vasopressin (AVP) has a dual action mainly in the periphery, ie, vasoconstriction and
water reabsorption via V 1A and V 2 receptors; it may play a role in a number of diseases, …