A Highly Effective Diels—Alder Approach to cis-Clerodane Natural Products: First Total Synthesis of Solidago Alcohol (I).

ChemInform ◽  
2004 ◽  
Vol 35 (26) ◽  
Author(s):  
Tai Wei Ly ◽  
Jyh-Hsiung Liao ◽  
Kak-Shan Shia ◽  
Hsing-Jang Liu
Synthesis ◽  
2004 ◽  
pp. 271-275 ◽  
Author(s):  
Hsing-Jang Liu ◽  
Tai Wei Ly ◽  
Jyh-Hsiung Liao ◽  
Kak-Shan Shia

Author(s):  
Mintu Munda ◽  
Sovan Niyogi ◽  
Kundan Shaw ◽  
Sourav Kundu ◽  
Rhituparna Nandi ◽  
...  

Electrochemical strategy has been the powerful approach for the synthesis of valuable intermediates, in particular heterocyclic motifs. It has proven to be an environmentally benign, highly effective and versatile platform...


ChemInform ◽  
2016 ◽  
Vol 47 (9) ◽  
pp. no-no
Author(s):  
Majid M. Heravi ◽  
Tahereh Ahmadi ◽  
Mahdieh Ghavidel ◽  
Bahareh Heidari ◽  
Hoda Hamidi

ChemInform ◽  
2010 ◽  
Vol 33 (48) ◽  
pp. no-no
Author(s):  
Yoshikazu Suzuki ◽  
Takeshi Murata ◽  
Ken-ichi Takao ◽  
Kin-ichi Tadano

RSC Advances ◽  
2015 ◽  
Vol 5 (123) ◽  
pp. 101999-102075 ◽  
Author(s):  
Majid M. Heravi ◽  
Tahereh Ahmadi ◽  
Mahdieh Ghavidel ◽  
Bahareh Heidari ◽  
Hoda Hamidi

The synthetic utility and potential power of the Diels–Alder (D–A) reaction in organic chemistry is evident.


1984 ◽  
Vol 62 (2) ◽  
pp. 183-234 ◽  
Author(s):  
Alex G. Fallis

Recent advances and examples of the intramolecular Diels–Alder reaction are summarized and applications to the total synthesis of natural products, both completed and in progress, noted. A detailed discussion of trienes leading to bicyclo[4.3.0]nonene skeletons is followed by examples of bicyclo[4.4.0]decenes and adducts arising from ortho-quinodimethane precursors. Cycloadditions affording bicyclo[n.4.0] systems and bridged-ring adducts from cyclic dienes conclude this survey which is followed by a discussion of unreactive trienes and a brief analysis of synthetic strategy to complete the review.


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