ChemInform Abstract: CHEMISTRY OF SINGLET OXYGEN. XXVII. DIRECTING EFFECT OF METHOXY GROUP IN ADDITIONS TO METHOXYSTYRENES

D. LERDAL; C. S. FOOTE

doi:10.1002/chin.197848247

ChemInform Abstract: CHEMISTRY OF SINGLET OXYGEN. XXVII. DIRECTING EFFECT OF METHOXY GROUP IN ADDITIONS TO METHOXYSTYRENES

Chemischer Informationsdienst ◽

10.1002/chin.197848247 ◽

1978 ◽

Vol 9 (48) ◽

Author(s):

D. LERDAL ◽

C. S. FOOTE

Keyword(s):

Singlet Oxygen ◽

Methoxy Group ◽

Directing Effect

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Chemistry of singlet Oxygen. XXVII. Directing effect of methoxy group in additions to methoxystyrenes

Tetrahedron Letters ◽

10.1016/s0040-4039(01)85600-8 ◽

1978 ◽

Vol 19 (35) ◽

pp. 3227-3230 ◽

Cited By ~ 36

Author(s):

Duane Lerdal ◽

Christopher S. Foote

Keyword(s):

Singlet Oxygen ◽

Methoxy Group ◽

Directing Effect

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Diastereoselective Photooxygenation of Chiral Naphthyl Alcohols: The Hydroxy Group Directing Effect in Singlet Oxygen [4+2] Cycloaddition to Arenes

Journal of the American Chemical Society ◽

10.1021/ja00130a006 ◽

1995 ◽

Vol 117 (25) ◽

pp. 6686-6690 ◽

Cited By ~ 17

Author(s):

Waldemar Adam ◽

Eva Maria Peters ◽

Karl Peters ◽

Michael Prein ◽

Hans Georg von Schnering

Keyword(s):

Singlet Oxygen ◽

Hydroxy Group ◽

Directing Effect

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π-Facial selectivity of the singlet oxygen [4+2] cycloaddition to chiral naphthalene derivatives: The directing effect of carbon-containing substituents

Tetrahedron ◽

10.1016/0040-4020(95)00812-m ◽

1995 ◽

Vol 51 (46) ◽

pp. 12583-12590 ◽

Cited By ~ 5

Author(s):

Waldemar Adam ◽

Michael Prein

Keyword(s):

Singlet Oxygen ◽

Naphthalene Derivatives ◽

Facial Selectivity ◽

Directing Effect

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Oxygenophilic organoaluminum-mediated conjugate addition of alkyllithium and Grignard reagents to quinone monoketals and quinol ethers. The directing effect of a methoxy group on the 1,4-addition process

The Journal of Organic Chemistry ◽

10.1021/jo00279a033 ◽

1989 ◽

Vol 54 (18) ◽

pp. 4413-4419 ◽

Cited By ~ 33

Author(s):

Alan J. Stern ◽

Jeffrey J. Rohde ◽

John S. Swenton

Keyword(s):

Methoxy Group ◽

Conjugate Addition ◽

Grignard Reagents ◽

Directing Effect

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ChemInform Abstract: Oxygenophilic Organoaluminum-Mediated Conjugate Addition of Alkyllithium and Grignard Reagents to Quinone Monoacetals and Quinol Ethers. The Directing Effect of a Methoxy Group on the 1,4-Addition Process.

ChemInform ◽

10.1002/chin.199006126 ◽

1990 ◽

Vol 21 (6) ◽

Author(s):

A. J. STERN ◽

J. J. ROHDE ◽

J. S. SWENTON

Keyword(s):

Methoxy Group ◽

Conjugate Addition ◽

Grignard Reagents ◽

Directing Effect

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ChemInform Abstract: π-Facial Selectivity of the Singlet Oxygen (4 + 2) Cycloaddition to Chiral Naphthalene Derivatives: The Directing Effect of Carbon- Containing Substituents.

ChemInform ◽

10.1002/chin.199611191 ◽

2010 ◽

Vol 27 (11) ◽

pp. no-no

Author(s):

W. ADAM ◽

M. PREIN

Keyword(s):

Singlet Oxygen ◽

Naphthalene Derivatives ◽

Facial Selectivity ◽

Directing Effect

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ChemInform Abstract: Diastereoselective Photooxygenation of Chiral Naphthyl Alcohols: The Hydroxy Group Directing Effect in Singlet Oxygen (4 + 2) Cycloaddition to Arenes.

ChemInform ◽

10.1002/chin.199543140 ◽

2010 ◽

Vol 26 (43) ◽

pp. no-no

Author(s):

W. ADAM ◽

E. M. PETERS ◽

K. PETERS ◽

M. PREIN ◽

H. G. VON SCHNERING

Keyword(s):

Singlet Oxygen ◽

Hydroxy Group ◽

Directing Effect

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Diastereoselective [4 + 2] cycloaddition of singlet oxygen in the photooxygenation of chiral naphthyl alcohols: evidence for a hydroxy group-directing effect

Journal of the American Chemical Society ◽

10.1021/ja00062a049 ◽

1993 ◽

Vol 115 (9) ◽

pp. 3766-3767 ◽

Cited By ~ 19

Author(s):

Waldemar Adam ◽

Michael Prein

Keyword(s):

Singlet Oxygen ◽

Hydroxy Group ◽

Directing Effect

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ChemInform Abstract: Diastereoselective (4 + 2) Cycloaddition of Singlet Oxygen in the Photooxygenation of Chiral Naphthyl Alcohols: Evidence for a Hydroxy Group-Directing Effect.

ChemInform ◽

10.1002/chin.199336064 ◽

2010 ◽

Vol 24 (36) ◽

pp. no-no

Author(s):

W. ADAM ◽

M. PREIN

Keyword(s):

Singlet Oxygen ◽

Hydroxy Group ◽

Directing Effect

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Singlet Oxygen in Synthesis. Formation of d,l- and meso-Isochrysohermidin from a 3,3′-Bipyrrole Precursor.

Tetrahedron ◽

10.1016/s0040-4020(97)00204-4 ◽

1997 ◽

Vol 53 (26) ◽

pp. 8731-8738

Author(s):

H Wasserman*

Keyword(s):

Singlet Oxygen

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