ChemInform Abstract: Studies on Chiral Organosulfur Compounds. Part 6. The Use of a Chiral Diene Bearing an Optically Active Sulfinylmethyl Group in the Lewis Acid-Catalyzed Intramolecular Asymmetric Hetero Diels-Alder Reaction.

K. HIROI; M. UMEMURA; Y. TOMIKAWA; M. KANEKO; F. KATO

doi:10.1002/chin.199745145

ChemInform Abstract: Studies on Chiral Organosulfur Compounds. Part 6. The Use of a Chiral Diene Bearing an Optically Active Sulfinylmethyl Group in the Lewis Acid-Catalyzed Intramolecular Asymmetric Hetero Diels-Alder Reaction.

ChemInform ◽

10.1002/chin.199745145 ◽

2010 ◽

Vol 28 (45) ◽

pp. no-no

Author(s):

K. HIROI ◽

M. UMEMURA ◽

Y. TOMIKAWA ◽

M. KANEKO ◽

F. KATO

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Optically Active ◽

Diels Alder ◽

Organosulfur Compounds ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

Studies on Chiral Organosulfur Compounds. VI. The Use of a Chiral Diene Bearing an Optically Active Sulfinylmethyl Group in the Lewis Acid-Catalyzed Intramolecular Asymmetric Hetero Diels-Alder Reaction.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.45.759 ◽

1997 ◽

Vol 45 (5) ◽

pp. 759-764 ◽

Cited By ~ 5

Author(s):

Kunio HIROI ◽

Masayuki UMEMURA ◽

Yoko TOMIKAWA ◽

Masamitsu KANEKO ◽

Fumiko KATO

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Optically Active ◽

Diels Alder ◽

Organosulfur Compounds ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

ChemInform Abstract: A Highly Asymmetric, Lewis Acid-Catalyzed Diels-Alder Reaction Using Optically Active 2-(3-Tolyl-p-sulfinyl)furyl α,β- Unsaturated Ketones as a Dienophile.

ChemInform ◽

10.1002/chin.199634107 ◽

2010 ◽

Vol 27 (34) ◽

pp. no-no

Author(s):

Y. ARAI ◽

T. MASUDA ◽

Y. MASAKI ◽

M. SHIRO

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Optically Active ◽

Diels Alder ◽

Unsaturated Ketones ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

ChemInform Abstract: The Lewis Acid-Catalyzed Intramolecular Asymmetric Hetero-Diels-Alder Reaction of Chiral α′-Sulfinyl α,β-Unsaturated Ketone. A Chiral Diene Bearing an Optically Active Sulfinylmethyl Group.

ChemInform ◽

10.1002/chin.199329151 ◽

2010 ◽

Vol 24 (29) ◽

pp. no-no

Author(s):

K. HIROI ◽

M. UMEMURA ◽

Y. TOMIKAWA

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Optically Active ◽

Diels Alder ◽

Unsaturated Ketone ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

The Lewis Acid-catalyzed Intramolecular Asymmetric Hetero Diels-Alder Reaction of Chiral a'-Sulfinyl-a,b-unsaturated Ketone. A Chiral Diene Bearing an Optically Active Sulfinylmethyl Group

Heterocycles ◽

10.3987/com-92-s27 ◽

1993 ◽

Vol 35 (1) ◽

pp. 73 ◽

Cited By ~ 7

Author(s):

Kunio Hiroi ◽

Masayuki Umemura ◽

Yoko Tomikawa

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Optically Active ◽

Diels Alder ◽

Unsaturated Ketone ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

Synthesis of Medium-Sized Carbocycles via a Bidentate Lewis Acid-Catalyzed Inverse Electron-Demand Diels–Alder Reaction Followed by Photoinduced Ring-Opening

Organic Letters ◽

10.1021/acs.orglett.1c00249 ◽

2021 ◽

Author(s):

Julia Ruhl ◽

Sebastian Ahles ◽

Marcel A. Strauss ◽

Christopher M. Leonhardt ◽

Hermann A. Wegner

Keyword(s):

Lewis Acid ◽

Ring Opening ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Acid Catalyzed ◽

Electron Demand

Download Full-text

Asymmetric synthesis of N-phenylethyl-2-phenyldecahydroquinolin-4-ones via Lewis acid catalyzed imino-Diels–Alder reaction

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)00201-9 ◽

2000 ◽

Vol 11 (12) ◽

pp. 2509-2523 ◽

Cited By ~ 3

Author(s):

Renée Paugam ◽

Emmanuelle Valenciennes ◽

Linda Le Coz-Bardol ◽

Jean-Christophe Garde ◽

Lya Wartski ◽

...

Keyword(s):

Asymmetric Synthesis ◽

Lewis Acid ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

On the lewis acid catalyzed diels-alder reaction of furan. regio- and stereospecific synthesis of substituted cyclohexenols and cyclohexadienols.

Tetrahedron Letters ◽

10.1016/s0040-4039(00)85823-2 ◽

1982 ◽

Vol 23 (50) ◽

pp. 5299-5302 ◽

Cited By ~ 111

Author(s):

Francis Brion

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Diels Alder ◽

Stereospecific Synthesis ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

ChemInform Abstract: TRANSITION STATE CONFORMATIONS OF A LEWIS ACID CATALYZED DIELS-ALDER REACTION. THE LOW TEMPERATURE CYCLOADDITION OF 1-(1-OXOALLYL)-2-(3-ISOPROPENYL-4-METHYL-3-PENTENYL) BENZENE

Chemischer Informationsdienst ◽

10.1002/chin.198547081 ◽

1985 ◽

Vol 16 (47) ◽

Author(s):

K. J. SHEA ◽

J. W. GILMAN

Keyword(s):

Low Temperature ◽

Transition State ◽

Lewis Acid ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

Trans-2-Diethylphosphoryloxy-1,3-Pentadiene in The Lewis acid Catalyzed Diels-Alder Reaction

Synthetic Communications ◽

10.1080/00397918608056399 ◽

1986 ◽

Vol 16 (12) ◽

pp. 1485-1492 ◽

Cited By ~ 4

Author(s):

Hsing-Jang Liu ◽

Waiseng Martin Feng

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text

Synthesis and in vitro cytotoxicity of 3-substituted-1,8-diazaanthraquinones produced by Lewis-acid catalyzed hetero diels-alder reaction

Bioorganic & Medicinal Chemistry Letters ◽

10.1016/s0960-894x(98)00543-5 ◽

1998 ◽

Vol 8 (21) ◽

pp. 2991-2994 ◽

Cited By ~ 13

Author(s):

Heesoon Lee ◽

Seung-Il Lee ◽

Sung-Il Yang

Keyword(s):

Lewis Acid ◽

Alder Reaction ◽

In Vitro Cytotoxicity ◽

Diels Alder ◽

Diels Alder Reaction ◽

Acid Catalyzed

Download Full-text