Tetrahedron Letters

First total synthesis of haplacutine C

N Kutsumura, K Numata, T Saito

Index: Kutsumura, Noriki; Kubokawa, Keisuke; Saito, Takao Synlett, 2010 , # 18 p. 2717 - 2720

Full Text: HTML

Citation Number: 0

Abstract

Abstract A total synthesis of haplacutine C has been achieved. The synthetic key features were the intramolecular aldol condensation for construction of the 4-quinolinone skeleton and the Stille coupling for elongation of the dienol side chain. In addition, the 4-O-protected-

Related Articles:

A practical preparation of terminal alkynes from aldehydes

[Wang, Zhe; Campagna, Silvio; Yang, Kaihong; Xu, Guoyou; Pierce, Michael E.; Fortunak, Joseph M.; Confalone, Pat N. Journal of Organic Chemistry, 2000 , vol. 65, # 6 p. 1889 - 1891]

Conversion of bromoalkenes into alkynes by wet tetra-n-butylammonium fluoride

[Okutani, Masaru; Mori, Yuji Journal of Organic Chemistry, 2009 , vol. 74, # 1 p. 442 - 444]

Thieme Chemistry Journal Awardees-Where are They Now? A General One-Step Synthesis of Alkynes from Enolisable Carbonyl Compounds

[Lyapkalo, Ilya M.; Vogel, Michael A. K.; Boltukhina, Ekaterina V.; Vavrik, Jiri Synlett, 2009 , # 4 p. 558 - 561]

Cs 2 CO 3-mediated synthesis of terminal alkynes from 1, 1-dibromo-1-alkenes

[Zhao, Ming; Kuang, Chunxiang; Yang, Qing; Cheng, Xuezhi Tetrahedron Letters, 2011 , vol. 52, # 9 p. 992 - 994]

TBAF-Promoted Elimination of Vicinal Dibromides Having an Adjacent O-Functional Group: Syntheses of 2-Bromoalk-1-enes and Alkynes

[Synthesis, , # 15 p. 2377 - 2382]

More Articles...