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Featured researches published by A. Yamashita.


Tetrahedron Letters | 1986

Synthesis of indenes from alkynes and phenyl amino chromium carbene complexes

A. Yamashita

Abstract Reactions of phenyl morpholino or pyrrolidino chromium carbene complexes with alkynes in DMF at 120–125°C resulted in exclusive formation of the indene derivatives.


Tetrahedron Letters | 1986

Regioselectivity of the reaction of a chromium-carbene complex with alkynes: Examination of steric and electronic factors

A. Yamashita; A. Toy

Abstract Examination of a steric and electronic factor of alkyne in regioselectivity in the reaction of a phenyl chromium carbene complex with unsymmetrical alkynes is described.


Tetrahedron Letters | 1982

Reaction of aryl chromium carbene complexes with ethyl propiolate a versatile vinyl ether formation

A. Yamashita; Terrence A. Scahill

Abstract Arylmethoxychromium-carbene complexes reacted with ethyl propiolate in the presence of alcohol to form and yields of aryl vinyl ether derivatives of malonate.


Tetrahedron Letters | 1985

Reaction of a pyrrole-carbene chromium complex with alkynes: a facile hydroindoloquinone formation with in-situ protection.

A. Yamashita; Terrence A. Scahill; A. Toy

Abstract Cycloaddition reaction of a pyrrole-carbene chromium complex with alkyne in the presence of acetic anhydride and triethylamine provided the acetylated hydroindoloquinone derivative.


Tetrahedron Letters | 1988

Synthesis of cyclopentanones via reaction of furan chromium carbene complexes with alkynes

A. Yamashita; A. Toy; William Watt; C.R. Muchmore

Abstract Reactions of the furan-methoxy chromium carbene complexes with alkynes in DMF at 120°C provided cyclopentafurans, which served as useful precursors for cyclopentanones and other ring systems.


Tetrahedron Letters | 1988

Reaction of aryl chromium carbene complexes with 1-hexyne; formation of unusual diels-alder cycloaddition products

A. Yamashita; J.M. Timko; William Watt

Abstract The reaction of an aryl chromium carbene complex with 1-hexyne provided a benzannulated product as a major component along with unusual Diels-Alder cycloaddition products.


Tetrahedron Letters | 1985

Reactions of aryl chromium carbene complexes with alkoxalkyne: O-Quinonemethide formation and unusual diels-alder dimerization

A. Yamashita; Terrence A. Scahill; Connie G. Chidester

Abstract Reactions of a pyrrole- and a phenyl-carbene chromium complexes with 3-alkoxy-1-ethoxy-1-butyne produced dimers through o-quinone-methide formation from the alkyne-carbene cycloaddition products and subsequent Diels-Alder dimerization.


Archive | 1986

Substituted naphthalenes, indoles, benzofurans, and benzothiophenes as lipoxygenase inhibitors

A. Yamashita; Herbert G. Johnson


Organic Syntheses | 2003

Synthesis of 2-Substituted Naphthalenediol Derivatives using Chromium Carbene Complexes: 1-Acetoxy-2-Butyl-4-Methoxynaphthalene

Joseph M. Timko; A. Yamashita


Archive | 1988

Intermediates for antiatherosclerotic furochromones

A. Yamashita

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