ChemInform Abstract: Guanacastepene, a Fungal-Derived Diterpene Antibiotic with a New Carbon Skeleton

Sean F. Brady; Maya P. Singh; Jeff E. Janso; Jon Clardy

doi:10.1002/chin.200022211

ChemInform Abstract: Guanacastepene, a Fungal-Derived Diterpene Antibiotic with a New Carbon Skeleton

ChemInform ◽

10.1002/chin.200022211 ◽

2010 ◽

Vol 31 (22) ◽

pp. no-no

Author(s):

Sean F. Brady ◽

Maya P. Singh ◽

Jeff E. Janso ◽

Jon Clardy

Keyword(s):

Carbon Skeleton ◽

Guanacastepene A

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Unique Strategy for the Assembly of the Carbon Skeleton of Guanacastepene A Using an Allenic Pauson−Khand-Type Reaction

Organic Letters ◽

10.1021/ol035322x ◽

2003 ◽

Vol 5 (19) ◽

pp. 3491-3494 ◽

Cited By ~ 71

Author(s):

Kay M. Brummond ◽

Dong Gao

Keyword(s):

Carbon Skeleton ◽

Type Reaction ◽

Guanacastepene A

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Progress towards the total synthesis of guanacastepene A. Approaches to the construction of quaternary carbons and the 5-7-6 tricyclic carbon skeleton

Tetrahedron Letters ◽

10.1016/s0040-4039(02)00729-3 ◽

2002 ◽

Vol 43 (22) ◽

pp. 4033-4036 ◽

Cited By ~ 26

Author(s):

Truc M. Nguyen ◽

Daesung Lee

Keyword(s):

Total Synthesis ◽

Carbon Skeleton ◽

Guanacastepene A ◽

Quaternary Carbons

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Guanacastepene, a Fungal-Derived Diterpene Antibiotic with a New Carbon Skeleton

Journal of the American Chemical Society ◽

10.1021/ja993835m ◽

2000 ◽

Vol 122 (9) ◽

pp. 2116-2117 ◽

Cited By ~ 118

Author(s):

Sean F. Brady ◽

Maya P. Singh ◽

Jeff E. Janso ◽

Jon Clardy

Keyword(s):

Carbon Skeleton ◽

Guanacastepene A

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On terpenes. LXXXIX. Direct proof of the carbon skeleton of germacrone

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19582169 ◽

1958 ◽

Vol 23 (12) ◽

pp. 2169-2174 ◽

Cited By ~ 8

Author(s):

V. Herout ◽

M. Suchý

Keyword(s):

Direct Proof ◽

Carbon Skeleton

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Fischdiabietane A, an Antitumoral Diterpenoid Dimer Featuring an Unprecedented Carbon Skeleton from Euphorbia fischeriana

The Journal of Organic Chemistry ◽

10.1021/acs.joc.1c00305 ◽

2021 ◽

Vol 86 (8) ◽

pp. 5894-5900

Author(s):

Jun He ◽

Jie-Kun Xu ◽

Lin-Bo Guo ◽

Cong-Yuan Xia ◽

Wen-Wen Lian ◽

...

Keyword(s):

Carbon Skeleton ◽

Euphorbia Fischeriana

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ChemInform Abstract: Azorellanol: A Diterpenoid with a New Carbon Skeleton from Azorella compacta.

ChemInform ◽

10.1002/chin.199919191 ◽

2010 ◽

Vol 30 (19) ◽

pp. no-no

Author(s):

Luis Alberto Loyola ◽

Jorge Borquez ◽

Glauco Morales ◽

Aurelio San-Martin ◽

Victor Manriquez ◽

...

Keyword(s):

Carbon Skeleton

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Total Synthesis of Stachyodin A via One-Pot Suzuki Coupling for Quick Construction of Carbon Skeleton

Organic Letters ◽

10.1021/acs.orglett.1c00998 ◽

2021 ◽

Author(s):

Yuichiro Kawamoto ◽

Toyoharu Kobayashi ◽

Hisanaka Ito

Keyword(s):

Total Synthesis ◽

Suzuki Coupling ◽

Carbon Skeleton ◽

One Pot

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Highly stable Na metal anode enabled by a multifunctional hard carbon skeleton

Carbon ◽

10.1016/j.carbon.2021.01.144 ◽

2021 ◽

Vol 176 ◽

pp. 219-227

Author(s):

Juli Liang ◽

Wenwei Wu ◽

Lin Xu ◽

Xuehang Wu

Keyword(s):

Carbon Skeleton ◽

Hard Carbon ◽

Metal Anode

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Air-engaged fabrication of nitrogen-doped carbon skeleton as an excellent platform for ultrafine well-dispersed RuNi alloy nanoparticles toward efficient hydrolysis of ammonia borane

Fuel ◽

10.1016/j.fuel.2021.120750 ◽

2021 ◽

Vol 297 ◽

pp. 120750

Author(s):

Yating He ◽

Yumei Peng ◽

Yi Wang ◽

Yan Long ◽

Guangyin Fan

Keyword(s):

Ammonia Borane ◽

Carbon Skeleton ◽

Alloy Nanoparticles ◽

Nitrogen Doped ◽

Nitrogen Doped Carbon ◽

Hydrolysis Of

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Stereoselective Convergent Synthesis of Carbon Skeleton of Cotylenin A Aglycone

Synthesis ◽

10.1055/s-0040-1706684 ◽

2021 ◽

Author(s):

Kazuyuki Sugita ◽

Motoi Kuwabara ◽

Ami Matsuo ◽

Shogo Kamo ◽

Akinobu Matsuzawa

Keyword(s):

Single Crystal ◽

Aldol Reaction ◽

Coupling Reaction ◽

Carbon Skeleton ◽

Convergent Synthesis ◽

X Ray ◽

Related Compounds

AbstractIn this paper, the synthesis of the carbon skeleton of cotylenin A aglycone is described. The key reactions, including an intramolecular aldol reaction, an aldol coupling reaction, and a ring-closing metathesis, allow for the effective and stereoselective access to the carbon skeleton of cotylenin A aglycone. The stereochemistry was confirmed by single-crystal X-ray crystallographic analyses of related compounds.

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