Concise Synthesis of Linderaspirone A and Bi‐linderone

Fenfen Xiao; Wu Liu; Yunxia Wang; Qing Zhang; Xiang Li; Xiangdong Hu

doi:10.1002/ajoc.201200184

Photogenic: The synthesis of linderaspirone A has been accomplished in only three steps by a Darzens cyclopentenedione synthesis and dioxygen‐assisted photochemical dimerization. Moreover, the thermal isomerization of linderaspirone A into bi‐linderone has been discovered, which may give clues to the biosynthetic pathway for bi‐linderone.

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References (56)

( S. Y. Wang , X. Y. Lan , J. H. Xiao , J. C. Yang , Y. T. Kao , S. T. Chang , Phytother. Res. 2008, 22, 213–216; 17726736)
S. Y. Wang , X. Y. Lan , J. H. Xiao , J. C. Yang , Y. T. Kao , S. T. Chang , Phytother. Res. 2008, 22, 213–216; 17726736
S. Y. Wang , X. Y. Lan , J. H. Xiao , J. C. Yang , Y. T. Kao , S. T. Chang , Phytother. Res. 2008, 22, 213–216; 17726736, S. Y. Wang , X. Y. Lan , J. H. Xiao , J. C. Yang , Y. T. Kao , S. T. Chang , Phytother. Res. 2008, 22, 213–216; 17726736
Fei Wang, Yuan Gao, Ling Zhang, Jikai Liu (2010)
Bi-linderone, a highly modified methyl-linderone dimer from Lindera aggregata with activity toward improvement of insulin sensitivity in vitro.
Organic letters, 12 10
( T. N. G. Row , H. R. Swamy , K. R. Acharya , V. Ramamurthy , K. Venkatesan , C. N. R. Rao , Tetrahedron Lett. 1983, 24, 3263–3266; )
T. N. G. Row , H. R. Swamy , K. R. Acharya , V. Ramamurthy , K. Venkatesan , C. N. R. Rao , Tetrahedron Lett. 1983, 24, 3263–3266;
T. N. G. Row , H. R. Swamy , K. R. Acharya , V. Ramamurthy , K. Venkatesan , C. N. R. Rao , Tetrahedron Lett. 1983, 24, 3263–3266; , T. N. G. Row , H. R. Swamy , K. R. Acharya , V. Ramamurthy , K. Venkatesan , C. N. R. Rao , Tetrahedron Lett. 1983, 24, 3263–3266;
T. Ohno, A. Nagatsu, Munehiro Nakagawa, M. Inoue, Yun-Mo Li, S. Minatoguchi, H. Mizukami, H. Fujiwara (2005)
New sesquiterpene lactones from water extract of the root of Lindera strychnifolia with cytotoxicity against the human small cell lung cancer cell, SBC-3
Tetrahedron Letters, 46
( A. K. Kiang , H. H. Lee , K. Y. Sim , J. Chem. Soc. 1962, 4338–4345.)
A. K. Kiang , H. H. Lee , K. Y. Sim , J. Chem. Soc. 1962, 4338–4345.
A. K. Kiang , H. H. Lee , K. Y. Sim , J. Chem. Soc. 1962, 4338–4345., A. K. Kiang , H. H. Lee , K. Y. Sim , J. Chem. Soc. 1962, 4338–4345.
( H. C. Kwon , N. I. Baek , S. U. Choi , K. R. Lee , Chem. Pharm. Bull. 2000, 48, 614–616; 10823695)
H. C. Kwon , N. I. Baek , S. U. Choi , K. R. Lee , Chem. Pharm. Bull. 2000, 48, 614–616; 10823695
H. C. Kwon , N. I. Baek , S. U. Choi , K. R. Lee , Chem. Pharm. Bull. 2000, 48, 614–616; 10823695, H. C. Kwon , N. I. Baek , S. U. Choi , K. R. Lee , Chem. Pharm. Bull. 2000, 48, 614–616; 10823695
Shi-you Li, Cong Chen, Hai-qing Zhang, Haizhou Guo, Hui Wang, Lin Wang, Xiang Zhang, Shi-neng Hua, Jun Yu, P. Xiao, Rong-Song Li, X. Tan (2005)
Identification of natural compounds with antiviral activities against SARS-associated coronavirus
Antiviral Research, 67
( N. G. Clemo , D. R. Gedge , G. Pattenden , J. Chem. Soc. Perkin Trans. 1 1981, 1448–1453.)
N. G. Clemo , D. R. Gedge , G. Pattenden , J. Chem. Soc. Perkin Trans. 1 1981, 1448–1453.
N. G. Clemo , D. R. Gedge , G. Pattenden , J. Chem. Soc. Perkin Trans. 1 1981, 1448–1453., N. G. Clemo , D. R. Gedge , G. Pattenden , J. Chem. Soc. Perkin Trans. 1 1981, 1448–1453.
J. Sweeney, A. Cantrill, M. Drew, A. McLaren, S. Thobhani (2006)
Asymmetric aziridine synthesis by aza-Darzens reaction of N-diphenylphosphinylimines with chiral enolates. Part 2: Inversion of diastereoselectivity
Tetrahedron, 62
A. Schwartz, P. Madan, E. Mohacsi, J. O'brien, L. Todaro, D. Coffen (1992)
Enantioselective synthesis of calcium channel blockers of the diltiazem group
Journal of Organic Chemistry, 57
( A. Schwartz , P. B. Madan , E. Mohacsi , J. P. O’Brien , L. J. Todaro , D. L. Coffen , J. Org. Chem. 1992, 57, 851–856; )
A. Schwartz , P. B. Madan , E. Mohacsi , J. P. O’Brien , L. J. Todaro , D. L. Coffen , J. Org. Chem. 1992, 57, 851–856;
A. Schwartz , P. B. Madan , E. Mohacsi , J. P. O’Brien , L. J. Todaro , D. L. Coffen , J. Org. Chem. 1992, 57, 851–856; , A. Schwartz , P. B. Madan , E. Mohacsi , J. P. O’Brien , L. J. Todaro , D. L. Coffen , J. Org. Chem. 1992, 57, 851–856;
( H. H. Lee , Y. T. Que , J. Chem. Soc. Perkin Trans. 1 1985, 453–455; )
H. H. Lee , Y. T. Que , J. Chem. Soc. Perkin Trans. 1 1985, 453–455;
H. H. Lee , Y. T. Que , J. Chem. Soc. Perkin Trans. 1 1985, 453–455; , H. H. Lee , Y. T. Que , J. Chem. Soc. Perkin Trans. 1 1985, 453–455;
( F. A. Davis , T. Ramachandar , Y. Wu , J. Org. Chem. 2003, 68, 6894–6898; 12946128)
F. A. Davis , T. Ramachandar , Y. Wu , J. Org. Chem. 2003, 68, 6894–6898; 12946128
F. A. Davis , T. Ramachandar , Y. Wu , J. Org. Chem. 2003, 68, 6894–6898; 12946128, F. A. Davis , T. Ramachandar , Y. Wu , J. Org. Chem. 2003, 68, 6894–6898; 12946128
( X. C. Li , D. Ferreira , M. R. Jacob , Q. Zhang , S. I. Khan , H. N. EI Sohly , D. G. Nagle , T. J. Smillie , I. A. Khan , L. A. Walker , A. M. Clark , J. Am. Chem. Soc. 2004, 126, 6872–6873; 15174849)
X. C. Li , D. Ferreira , M. R. Jacob , Q. Zhang , S. I. Khan , H. N. EI Sohly , D. G. Nagle , T. J. Smillie , I. A. Khan , L. A. Walker , A. M. Clark , J. Am. Chem. Soc. 2004, 126, 6872–6873; 15174849
X. C. Li , D. Ferreira , M. R. Jacob , Q. Zhang , S. I. Khan , H. N. EI Sohly , D. G. Nagle , T. J. Smillie , I. A. Khan , L. A. Walker , A. M. Clark , J. Am. Chem. Soc. 2004, 126, 6872–6873; 15174849, X. C. Li , D. Ferreira , M. R. Jacob , Q. Zhang , S. I. Khan , H. N. EI Sohly , D. G. Nagle , T. J. Smillie , I. A. Khan , L. A. Walker , A. M. Clark , J. Am. Chem. Soc. 2004, 126, 6872–6873; 15174849
D. Aldous, Anne Dalençon, P. Steel (2002)
A short synthesis of (+/-)-epiasarinin.
Organic letters, 4 7
Y. Aoyama, T. Konoike, A. Kanda, N. Naya, M. Nakajima (2001)
Total synthesis of human chymase inhibitor methyllinderone and structure--activity relationships of its derivatives.
Bioorganic & medicinal chemistry letters, 11 13
F. Davis, T. Ramachandar, Yongzhong Wu (2003)
Improved asymmetric synthesis of aziridine 2-phosphonates using (S)-(+)-2,4,6-trimethylphenylsulfinamide.
The Journal of organic chemistry, 68 18
( G. Bose , P. Langer , Synlett 2005, 6, 1021–1023; )
G. Bose , P. Langer , Synlett 2005, 6, 1021–1023;
G. Bose , P. Langer , Synlett 2005, 6, 1021–1023; , G. Bose , P. Langer , Synlett 2005, 6, 1021–1023;
N. Clemo, D. Gedge, G. Pattenden (1981)
Synthesis of calythrone and related cyclopentene-1,3-diones via rearrangement of 4-ylidenebutenolides
Journal of The Chemical Society-perkin Transactions 1, 12
( I. Inhülsen , K. Chin , M. Göwert , P. Margaretha , Helv. Chim. Acta 2011, 94, 1030–1034.)
I. Inhülsen , K. Chin , M. Göwert , P. Margaretha , Helv. Chim. Acta 2011, 94, 1030–1034.
I. Inhülsen , K. Chin , M. Göwert , P. Margaretha , Helv. Chim. Acta 2011, 94, 1030–1034., I. Inhülsen , K. Chin , M. Göwert , P. Margaretha , Helv. Chim. Acta 2011, 94, 1030–1034.
( N. Y. Wang , S. Minatoguchi , M. Arai , Y. Uno , K. Hashimoto , X. H. Chen , K. Fukuda , S. Akao , G. Takemura , H. Fujiwara , Am. J. Chin. Med. 2004, 32, 587–598.15481648)
N. Y. Wang , S. Minatoguchi , M. Arai , Y. Uno , K. Hashimoto , X. H. Chen , K. Fukuda , S. Akao , G. Takemura , H. Fujiwara , Am. J. Chin. Med. 2004, 32, 587–598.15481648
N. Y. Wang , S. Minatoguchi , M. Arai , Y. Uno , K. Hashimoto , X. H. Chen , K. Fukuda , S. Akao , G. Takemura , H. Fujiwara , Am. J. Chin. Med. 2004, 32, 587–598.15481648, N. Y. Wang , S. Minatoguchi , M. Arai , Y. Uno , K. Hashimoto , X. H. Chen , K. Fukuda , S. Akao , G. Takemura , H. Fujiwara , Am. J. Chin. Med. 2004, 32, 587–598.15481648
The corresponding alpha-chloro/iodo ketones gave worse results. Please see the Supporting Information for details
Hiok-Huang Lee, Y. Que, S. Ng (1985)
Synthesis of lucidones
Journal of The Chemical Society-perkin Transactions 1, 16
( M. Kozuka , M. Yoshikawa , T. Sawada , J. Nat. Prod. 1984, 47, 1063–1063.6533267)
M. Kozuka , M. Yoshikawa , T. Sawada , J. Nat. Prod. 1984, 47, 1063–1063.6533267
M. Kozuka , M. Yoshikawa , T. Sawada , J. Nat. Prod. 1984, 47, 1063–1063.6533267, M. Kozuka , M. Yoshikawa , T. Sawada , J. Nat. Prod. 1984, 47, 1063–1063.6533267
( G. J. Bennett , H. H. Lee , J. Chem. Soc. Perkin Trans. 1 1986, 633–638; )
G. J. Bennett , H. H. Lee , J. Chem. Soc. Perkin Trans. 1 1986, 633–638;
G. J. Bennett , H. H. Lee , J. Chem. Soc. Perkin Trans. 1 1986, 633–638; , G. J. Bennett , H. H. Lee , J. Chem. Soc. Perkin Trans. 1 1986, 633–638;
The new approach to methyl linderone is the subject of an application for a Chinese Patent
( D. J. Aldous , A. J. Dalencon , P. G. Steel , Org. Lett. 2002, 4, 1159–1162; 11922807)
D. J. Aldous , A. J. Dalencon , P. G. Steel , Org. Lett. 2002, 4, 1159–1162; 11922807
D. J. Aldous , A. J. Dalencon , P. G. Steel , Org. Lett. 2002, 4, 1159–1162; 11922807, D. J. Aldous , A. J. Dalencon , P. G. Steel , Org. Lett. 2002, 4, 1159–1162; 11922807
Inga Inhülsen, K. Chin, Maren Göwert, P. Margaretha (2011)
Photocycloaddition of 4‐(Alk‐1‐ynyl)‐Substituted Coumarins and Thiocoumarins to 2,3‐Dimethylbuta‐1,3‐diene
Helvetica Chimica Acta, 94
Fei Wang, Yuan Gao, Ling Zhang, Bing Bai, Yaowen Hu, Zejun Dong, Qingfeng Zhai, Hua-Jie Zhu, Ji Liu (2010)
A pair of windmill-shaped enantiomers from Lindera aggregata with activity toward improvement of insulin sensitivity.
Organic letters, 12 14
( C. F. Zhang , Q. S. Sun , Y. Y. Zhao , Z. T. Wang , Chin. J. Med. Chem. 2001, 11, 274–276; )
C. F. Zhang , Q. S. Sun , Y. Y. Zhao , Z. T. Wang , Chin. J. Med. Chem. 2001, 11, 274–276;
C. F. Zhang , Q. S. Sun , Y. Y. Zhao , Z. T. Wang , Chin. J. Med. Chem. 2001, 11, 274–276; , C. F. Zhang , Q. S. Sun , Y. Y. Zhao , Z. T. Wang , Chin. J. Med. Chem. 2001, 11, 274–276;
( Y. Onizawa , H. Kusama , N. Iwasawa , J. Am. Chem. Soc. 2008, 130, 802–803.18154295)
Y. Onizawa , H. Kusama , N. Iwasawa , J. Am. Chem. Soc. 2008, 130, 802–803.18154295
Y. Onizawa , H. Kusama , N. Iwasawa , J. Am. Chem. Soc. 2008, 130, 802–803.18154295, Y. Onizawa , H. Kusama , N. Iwasawa , J. Am. Chem. Soc. 2008, 130, 802–803.18154295
A. Kiang, H. Lee, K. Sim (1962)
843. The structure of linderone and methyl-linderone
Journal of The Chemical Society (resumed)
Su-Yen Chang, M. Cheng, C. Peng, Hsun-Shuo Chang, I. Chen (2008)
Antimycobacterial Butanolides from the Root of Lindera akoensis
Chemistry & Biodiversity, 5
( J. B. Sweeney , A. A. Cantrill , M. G. B. Drew , A. B. McLAaren , S. Thobhani , Tetrahedron 2006, 62, 3694–3703; )
J. B. Sweeney , A. A. Cantrill , M. G. B. Drew , A. B. McLAaren , S. Thobhani , Tetrahedron 2006, 62, 3694–3703;
J. B. Sweeney , A. A. Cantrill , M. G. B. Drew , A. B. McLAaren , S. Thobhani , Tetrahedron 2006, 62, 3694–3703; , J. B. Sweeney , A. A. Cantrill , M. G. B. Drew , A. B. McLAaren , S. Thobhani , Tetrahedron 2006, 62, 3694–3703;
( L. S. Gan , Y. L. Zheng , J. M. Mo , X. Liu , X. H. Li , C. X. Zhou , J. Nat. Prod. 2009, 72, 1497–1501; 19639966)
L. S. Gan , Y. L. Zheng , J. M. Mo , X. Liu , X. H. Li , C. X. Zhou , J. Nat. Prod. 2009, 72, 1497–1501; 19639966
L. S. Gan , Y. L. Zheng , J. M. Mo , X. Liu , X. H. Li , C. X. Zhou , J. Nat. Prod. 2009, 72, 1497–1501; 19639966, L. S. Gan , Y. L. Zheng , J. M. Mo , X. Liu , X. H. Li , C. X. Zhou , J. Nat. Prod. 2009, 72, 1497–1501; 19639966
T. Row, H. Swamy, K. Acharya, V. Ramamurthy, K. Venkatesan, C. Rao (1983)
Reversible photodimerization of phenylbutadienes in the solid state
Tetrahedron Letters, 24
J. Deyrup (1969)
Darzens aziridine synthesis
Journal of Organic Chemistry, 34
( G. Q. Wang , K. Wei , L. Zhang , T. Feng , F. Wang , Q. A. Wang , J. K. Liu , Tetrahedron Lett. 2011, 52, 2719–2721.)
G. Q. Wang , K. Wei , L. Zhang , T. Feng , F. Wang , Q. A. Wang , J. K. Liu , Tetrahedron Lett. 2011, 52, 2719–2721.
G. Q. Wang , K. Wei , L. Zhang , T. Feng , F. Wang , Q. A. Wang , J. K. Liu , Tetrahedron Lett. 2011, 52, 2719–2721., G. Q. Wang , K. Wei , L. Zhang , T. Feng , F. Wang , Q. A. Wang , J. K. Liu , Tetrahedron Lett. 2011, 52, 2719–2721.
Xing-Cong Li, D. Ferreira, M. Jacob, Qifeng Zhang, Shabana Khan, H. Elsohly, D. Nagle, T. Smillie, I. Khan, L. Walker, A. Clark (2004)
Antifungal cyclopentenediones from Piper coruscans.
Journal of the American Chemical Society, 126 22
H. Kwon, N. Baek, S. Choi, K. Lee (2000)
New cytotoxic butanolides from Lindera obtusiloba BLUME.
Chemical & pharmaceutical bulletin, 48 5
Yuji Onizawa, H. Kusama, N. Iwasawa (2008)
Efficient control of pi-alkyne and vinylidene complex pathways for the W(CO)5(L)-catalyzed synthesis of two types of nitrogen-containing bicyclic compounds.
Journal of the American Chemical Society, 130 3
( F. Wang , Y. Gao , L. Zhang , B. Bai , Y. N. Hu , Z. J. Dong , Q. W. Zhai , H. J. Zhu , J. K. Liu , Org. Lett. 2010, 12, 3196–3199.20545338)
F. Wang , Y. Gao , L. Zhang , B. Bai , Y. N. Hu , Z. J. Dong , Q. W. Zhai , H. J. Zhu , J. K. Liu , Org. Lett. 2010, 12, 3196–3199.20545338
F. Wang , Y. Gao , L. Zhang , B. Bai , Y. N. Hu , Z. J. Dong , Q. W. Zhai , H. J. Zhu , J. K. Liu , Org. Lett. 2010, 12, 3196–3199.20545338, F. Wang , Y. Gao , L. Zhang , B. Bai , Y. N. Hu , Z. J. Dong , Q. W. Zhai , H. J. Zhu , J. K. Liu , Org. Lett. 2010, 12, 3196–3199.20545338
T. Ohno, G. Takemura, I. Murata, T. Kagawa, S. Akao, S. Minatoguchi, T. Fujiwara, H. Fujiwara (2005)
Water extract of the root of Lindera strychnifolia slows down the progression of diabetic nephropathy in db/db mice.
Life sciences, 77 12
( H. Tan , C. Zheng , Z. Liu , D. Z. Wang , Org. Lett. 2011, 13, 2192–2195.21446662)
H. Tan , C. Zheng , Z. Liu , D. Z. Wang , Org. Lett. 2011, 13, 2192–2195.21446662
H. Tan , C. Zheng , Z. Liu , D. Z. Wang , Org. Lett. 2011, 13, 2192–2195.21446662, H. Tan , C. Zheng , Z. Liu , D. Z. Wang , Org. Lett. 2011, 13, 2192–2195.21446662
( L. H. Gu , T. Wu , Z. J. Zhang , G. X. Chou , Z. T. Wang , Acta Pharm. Sin. 2006, 41, 956–962.)
L. H. Gu , T. Wu , Z. J. Zhang , G. X. Chou , Z. T. Wang , Acta Pharm. Sin. 2006, 41, 956–962.
L. H. Gu , T. Wu , Z. J. Zhang , G. X. Chou , Z. T. Wang , Acta Pharm. Sin. 2006, 41, 956–962., L. H. Gu , T. Wu , Z. J. Zhang , G. X. Chou , Z. T. Wang , Acta Pharm. Sin. 2006, 41, 956–962.
(The new approach to methyl linderone is the subject of an application for a Chinese Patent (no. 201110267743.1).)
The new approach to methyl linderone is the subject of an application for a Chinese Patent (no. 201110267743.1).
The new approach to methyl linderone is the subject of an application for a Chinese Patent (no. 201110267743.1)., The new approach to methyl linderone is the subject of an application for a Chinese Patent (no. 201110267743.1).
Sheng-Yang Wang, Xingyu Lan, Jun-Hong Xiao, Jen Yang, Yi-Ting Kao, Shang-Tzen Chang (2008)
Antiinflammatory activity of Lindera erythrocarpa fruits
Phytotherapy Research, 22
( J. A. Deyrup , J. Org. Chem. 1969, 34, 2724–2727.)
J. A. Deyrup , J. Org. Chem. 1969, 34, 2724–2727.
J. A. Deyrup , J. Org. Chem. 1969, 34, 2724–2727., J. A. Deyrup , J. Org. Chem. 1969, 34, 2724–2727.
M. Kozuka, M. Yoshikawa, T. Sawada (1984)
Alkaloids from Lindera strychnifolia.
Journal of natural products, 47 6
Ningyuan Wang, S. Minatoguchi, M. Arai, Y. Uno, K. Hashimoto, Chen Xue-Hai, K. Fukuda, S. Akao, G. Takemura, H. Fujiwara (2004)
Lindera strychnifolia is protective against post-ischemic myocardial dysfunction through scavenging hydroxyl radicals and opening the mitochondrial KATP channels in isolated rat hearts.
The American journal of Chinese medicine, 32 4
Gang-qiang Wang, Kun Wei, Lin Zhang, Tao Feng, Fei Wang, Qiu-an Wang, Jikai Liu (2011)
One-step biomimetic synthesis of (+/-)-linderaspirone A and (+/-)-bi-linderone
Tetrahedron Letters, 52
L. Gan, Y. Zheng, Jianxia Mo, Xin Liu, Xin Li, Chang‐xin Zhou (2009)
Sesquiterpene lactones from the root tubers of Lindera aggregata.
Journal of natural products, 72 8
G. Bennett, Hiok-Huang Lee (1986)
Oxidative rearrangement of quinochalcones. Part 2. A facile synthesis of linderone
Journal of The Chemical Society-perkin Transactions 1, 17
(The metal halide lamp (400 W) was purchased from Xian Bilon Biological Technology Co., Ltd. in China. Please see the Supporting Information for the relative spectral energy distribution curve of the lamp.)
The metal halide lamp (400 W) was purchased from Xian Bilon Biological Technology Co., Ltd. in China. Please see the Supporting Information for the relative spectral energy distribution curve of the lamp.
The metal halide lamp (400 W) was purchased from Xian Bilon Biological Technology Co., Ltd. in China. Please see the Supporting Information for the relative spectral energy distribution curve of the lamp., The metal halide lamp (400 W) was purchased from Xian Bilon Biological Technology Co., Ltd. in China. Please see the Supporting Information for the relative spectral energy distribution curve of the lamp.
Haibo Tan, C. Zheng, Zheng Liu, David Wang (2011)
Biomimetic total syntheses of linderaspirone A and bi-linderone and revisions of their biosynthetic pathways.
Organic letters, 13 9
( T. Ohno , G. Takemura , I. Murata , T. Kagawa , S. Akao , S. Minatoguchi , T. Fujiwara , H. Fujiwara , Life Sci. 2005, 77, 1391–1403.15925389)
T. Ohno , G. Takemura , I. Murata , T. Kagawa , S. Akao , S. Minatoguchi , T. Fujiwara , H. Fujiwara , Life Sci. 2005, 77, 1391–1403.15925389
T. Ohno , G. Takemura , I. Murata , T. Kagawa , S. Akao , S. Minatoguchi , T. Fujiwara , H. Fujiwara , Life Sci. 2005, 77, 1391–1403.15925389, T. Ohno , G. Takemura , I. Murata , T. Kagawa , S. Akao , S. Minatoguchi , T. Fujiwara , H. Fujiwara , Life Sci. 2005, 77, 1391–1403.15925389

Publisher: Wiley
ISSN: 2193-5807
eISSN: 2193-5815
DOI: 10.1002/ajoc.201200184
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Concise Synthesis of Linderaspirone A and Bi‐linderone

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Concise Synthesis of Linderaspirone A and Bi‐linderone

Concise Synthesis of Linderaspirone A and Bi‐linderone

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