Polyketide Assembly by Alkene−Alkyne Reductive Cross-Coupling: Spiroketals through the Union of Homoallylic Alcohols

Daniel P. Canterbury; Glenn C. Micalizio

doi:10.1021/ja102888f

Polyketide Assembly by Alkene−Alkyne Reductive Cross-Coupling: Spiroketals through the Union of Homoallylic Alcohols

Journal of the American Chemical Society ◽

10.1021/ja102888f ◽

2010 ◽

Vol 132 (22) ◽

pp. 7602-7604 ◽

Cited By ~ 28

Author(s):

Daniel P. Canterbury ◽

Glenn C. Micalizio

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols

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ChemInform Abstract: Intramolecular Hydrosilylation and Silicon-Assisted Cross-Coupling: An Efficient Route to Trisubstituted Homoallylic Alcohols.

ChemInform ◽

10.1002/chin.200118057 ◽

2001 ◽

Vol 32 (18) ◽

pp. no-no

Author(s):

Scott E. Denmark ◽

Weitao Pan

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols ◽

Efficient Route

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Cross-coupling of homoallylic alcohols with styrene

Tetrahedron Letters ◽

10.1016/j.tetlet.2010.08.054 ◽

2010 ◽

Vol 51 (42) ◽

pp. 5571-5573 ◽

Cited By ~ 4

Author(s):

Madhesan Balakrishnan ◽

Jin Kun Cha

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols

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Cobalt-Catalyzed Cross-Coupling Route to Homoallylic Alcohols and Amines

Synfacts ◽

10.1055/s-0036-1589270 ◽

2016 ◽

Vol 12 (10) ◽

pp. 1019-1019

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols

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ChemInform Abstract: Polyketide Assembly by Alkene-Alkyne Reductive Cross-Coupling: Spiroketals Through the Union of Homoallylic Alcohols.

ChemInform ◽

10.1002/chin.201041122 ◽

2010 ◽

Vol 41 (41) ◽

pp. no-no

Author(s):

Daniel P. Canterbury ◽

Glenn C. Micalizio

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols

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Intramolecular Anti-Hydrosilylation and Silicon-Assisted Cross-Coupling: Highly Regio- and Stereoselective Synthesis of Trisubstituted Homoallylic Alcohols

Organic Letters ◽

10.1021/ol026933c ◽

2002 ◽

Vol 4 (23) ◽

pp. 4163-4166 ◽

Cited By ~ 57

Author(s):

Scott E. Denmark ◽

Weitao Pan

Keyword(s):

Stereoselective Synthesis ◽

Cross Coupling ◽

Homoallylic Alcohols

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Concerning the potential reversibility of carbometalation in alkoxide-directed Ti(Oi-Pr)4-mediated reductive cross-coupling of homoallylic alcohols with aromatic imines

Chemical Communications ◽

10.1039/b927430h ◽

2010 ◽

Vol 46 (19) ◽

pp. 3336 ◽

Cited By ~ 8

Author(s):

Masayuki Takahashi ◽

Glenn C. Micalizio

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols ◽

Aromatic Imines

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Intramolecular Hydrosilylation and Silicon-Assisted Cross-Coupling: An Efficient Route to Trisubstituted Homoallylic Alcohols

Organic Letters ◽

10.1021/ol006769y ◽

2001 ◽

Vol 3 (1) ◽

pp. 61-64 ◽

Cited By ~ 76

Author(s):

Scott E. Denmark ◽

Weitao Pan

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols ◽

Efficient Route

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Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols

RSC Advances ◽

10.1039/c8ra09048c ◽

2018 ◽

Vol 8 (72) ◽

pp. 41561-41565 ◽

Cited By ~ 4

Author(s):

Xiao-Yu Lu ◽

Jin-Song Li ◽

Jin-Yu Wang ◽

Shi-Qun Wang ◽

Yue-Ming Li ◽

...

Keyword(s):

Cross Coupling ◽

Coupling Reactions ◽

Organoboron Compounds ◽

Cross Coupling Reactions ◽

Homoallylic Alcohols ◽

Vinyl Epoxide

Copper-catalyzed cross-coupling reactions of vinyl epoxide with arylboronates to obtain aryl-substituted homoallylic alcohols are described.

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ChemInform Abstract: Synthesis of Homoallylic Alcohols (III), (IV), (VI), (VII) via Palladium-Catalyzed Cross-Coupling of Vinylic Oxetanes (II) and Aryl and Vinylic Iodides or Triflates (I), (V).

ChemInform ◽

10.1002/chin.199416087 ◽

2010 ◽

Vol 25 (16) ◽

pp. no-no

Author(s):

R. C. LAROCK ◽

S. DING ◽

C. TU

Keyword(s):

Cross Coupling ◽

Homoallylic Alcohols ◽

Palladium Catalyzed

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Intramolecular anti-Hydrosilylation and Silicon-Assisted Cross-Coupling: Highly Regio- and Stereoselective Synthesis of Trisubstituted Homoallylic Alcohols.

ChemInform ◽

10.1002/chin.200313081 ◽

2003 ◽

Vol 34 (13) ◽

Author(s):

Scott E. Denmark ◽

Weitao Pan

Keyword(s):

Stereoselective Synthesis ◽

Cross Coupling ◽

Homoallylic Alcohols

Download Full-text