A General Strategy for the Construction of Calyciphylline A type Alkaloids: Divergent Total Syntheses of (–)‐Daphenylline and (–)‐Himalensine A

A General Strategy for Synthesis of Both (6Z)- and (6E)-Cladiellin Diterpenes: Total Syntheses of (−)-Cladiella-6,11-dien-3-ol, (+)-Polyanthellin A, (−)-Cladiell-11-ene-3,6,7-triol, and (−)-Deacetoxyalcyonin Acetate

Journal of the American Chemical Society ◽

10.1021/ja065782w ◽

2006 ◽

Vol 128 (49) ◽

pp. 15851-15855 ◽

Cited By ~ 44

Author(s):

Hyoungsu Kim ◽

Hyunjoo Lee ◽

Jayoung Kim ◽

Sanghee Kim ◽

Deukjoon Kim

Keyword(s):

General Strategy ◽

Total Syntheses

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ChemInform Abstract: GENERAL STRATEGY FOR GIBBERELLIN SYNTHESIS: TOTAL SYNTHESES OF (.+-.)-GIBBERELLIN A1 AND GIBBERELLIC ACID

Chemischer Informationsdienst ◽

10.1002/chin.198104347 ◽

1981 ◽

Vol 12 (4) ◽

Author(s):

L. LOMBARDO ◽

L. N. MANDER ◽

J. V. TURNER

Keyword(s):

Gibberellic Acid ◽

General Strategy ◽

Total Syntheses ◽

Gibberellin A1

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ChemInform Abstract: A General Strategy for the Synthesis of Cladiellin Diterpenes: Enantioselective Total Syntheses of 6-Acetoxycladiell-7(16),11-dien-3-ol (Deacetoxyalcyonin Acetate) (I), Cladiell-11-ene-3,6,7-triol (II), Sclerophytin A (III), and the I

ChemInform ◽

10.1002/chin.200204186 ◽

2010 ◽

Vol 33 (4) ◽

pp. no-no

Author(s):

David W. C. MacMillan ◽

Larry E. Overman ◽

Lewis D. Pennington

Keyword(s):

General Strategy ◽

Total Syntheses ◽

Sclerophytin A

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A General Strategy for the Construction of Calyciphylline A‐Type Alkaloids: Divergent Total Syntheses of (−)‐Daphenylline and (−)‐Himalensine A

Angewandte Chemie ◽

10.1002/ange.202016212 ◽

2021 ◽

Vol 133 (17) ◽

pp. 9525-9529

Author(s):

Bingyang Wang ◽

Bo Xu ◽

Wen Xun ◽

Yiming Guo ◽

Jing Zhang ◽

...

Keyword(s):

General Strategy ◽

Total Syntheses

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General strategy for gibberellin synthesis: total syntheses of (.+-.)-gibberellin A1 and gibberellic acid

Journal of the American Chemical Society ◽

10.1021/ja00541a071 ◽

1980 ◽

Vol 102 (21) ◽

pp. 6626-6628 ◽

Cited By ~ 49

Author(s):

Luciano Lombardo ◽

Lewis N. Mander ◽

John V. Turner

Keyword(s):

Gibberellic Acid ◽

General Strategy ◽

Total Syntheses ◽

Gibberellin A1

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Total Syntheses of Multiple Cladiellin Natural Products by Use of a Completely General Strategy

The Journal of Organic Chemistry ◽

10.1021/jo302542h ◽

2012 ◽

Vol 78 (2) ◽

pp. 673-696 ◽

Cited By ~ 26

Author(s):

J. Stephen Clark ◽

Raphaëlle Berger ◽

Stewart T. Hayes ◽

Hans Martin Senn ◽

Louis J. Farrugia ◽

...

Keyword(s):

Natural Products ◽

General Strategy ◽

Total Syntheses

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A General Strategy for the Synthesis of Cladiellin Diterpenes: Enantioselective Total Syntheses of 6-Acetoxycladiell-7(16),11-dien-3-ol (Deacetoxyalcyonin Acetate), Cladiell-11-ene-3,6,7-triol, Sclerophytin A, and the Initially Purported Structure of Sclerophytin A

Journal of the American Chemical Society ◽

10.1021/ja016351a ◽

2001 ◽

Vol 123 (37) ◽

pp. 9033-9044 ◽

Cited By ~ 73

Author(s):

David W. C. MacMillan ◽

Larry E. Overman ◽

Lewis D. Pennington

Keyword(s):

General Strategy ◽

Total Syntheses ◽

Sclerophytin A

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General Strategy for the Synthesis of Antirhine Alkaloids: Divergent Total Syntheses of (±)-Antirhine, (±)-18,19-Dihydroantirhine, and Their 20-Epimers

Organic Letters ◽

10.1021/acs.orglett.0c00544 ◽

2020 ◽

Vol 22 (6) ◽

pp. 2354-2358 ◽

Cited By ~ 2

Author(s):

Cheolwoo Bae ◽

Eunjoon Park ◽

Cheon-Gyu Cho ◽

Cheol-Hong Cheon

Keyword(s):

General Strategy ◽

Total Syntheses

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A General Strategy for Synthesis of Both (6Z)- and (6E)-Cladiellin Diterpenes: Total Syntheses of (-)-Cladiella-6,11-dien-3-ol (I), (+)-Polyanthellin A (II), (-)-Cladiell-11-ene-3,6,7-triol (III), and (-)-Deacetoxyalcyonin Acetate (IV).

ChemInform ◽

10.1002/chin.200716178 ◽

2007 ◽

Vol 38 (16) ◽

Author(s):

Hyoungsu Kim ◽

Hyunjoo Lee ◽

Jayoung Kim ◽

Sanghee Kim ◽

Deukjoon Kim

Keyword(s):

General Strategy ◽

Total Syntheses

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Stereoselective SE2‘ Additions of Enantioenriched Allylic Tin and Indium Reagents to Protected Threose and Erythrose Aldehydes: A General Strategy for the Stereocontrolled Synthesis of Precursors to the Eight Diastereomeric Hexoses and Their Enantiomers

The Journal of Organic Chemistry ◽

10.1021/jo9640231 ◽

1996 ◽

Vol 61 (25) ◽

pp. 9072-9072

Author(s):

James A. Marshall ◽

Kevin W. Hinkle

Keyword(s):

General Strategy ◽

Stereocontrolled Synthesis

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