Stereoselective route to functionalized cis-hydrindanes from tricyclo[5.2.1.02,6]decan-10-ones. A total synthesis of (±)-coronafacic acid

1993 ◽  
pp. 1573-1575 ◽  
Author(s):  
Goverdhan Mehta ◽  
Marapaka Praveen
Keyword(s):  
Total Synthesis ◽  
Coronafacic Acid

Total synthesis of d,l-coronafacic acid by an intermolecular Diels–Alder approach

1984 ◽  
Vol 62 (9) ◽  
pp. 1747-1750 ◽  
Author(s):  
Hsing-Jang Liu ◽  
Montse Llinas-Brunet
Keyword(s):  
Total Synthesis ◽  
Diels Alder ◽  
Keto Ester ◽  
Coronafacic Acid

An efficient total synthesis of d,l-coronafacic acid (2) has been achieved from 4-cyclopentene-1,3-dione (4). The synthesis involves keto ester 7 as a key intermediate that is conveniently prepared by the Diels–Alder addition of enedione 4 to ethyl 4-ethyl-2,4-pentadienoate (5).

TOTAL SYNTHESIS OF (±)-CORONAFACIC ACID

1981 ◽  
Vol 10 (6) ◽  
pp. 731-732 ◽  
Author(s):  
Mitsuru Nakayama ◽  
Susumu Ohira ◽  
Yuichi Okamura ◽  
Shinji Soga
Keyword(s):  
Total Synthesis ◽  
Coronafacic Acid

ChemInform Abstract: TOTAL SYNTHESIS OF (.+-.)-CORONAFACIC ACID

1981 ◽  
Vol 12 (49) ◽  
Author(s):  
M. NAKAYAMA ◽  
S. OHIRA ◽  
Y. OKAMURA ◽  
S. SOGA
Keyword(s):  
Total Synthesis ◽  
Coronafacic Acid

scholarly journals Total synthesis of (+)- and (-)-coronafacic acid.

1983 ◽  
Vol 47 (7) ◽  
pp. 1689-1690 ◽  
Author(s):  
Mitsuru NAKAYAMA ◽  
Susumu OHIRA
Keyword(s):  
Total Synthesis ◽  
Coronafacic Acid
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