ChemInform Abstract: Cs2.5H0.5PW12O40 Catalyzed Diastereoselective Synthesis of β-Amino Ketones via Three Component Mannich-Type Reaction in Water.

Type Reaction ◽

Cs2.5H0.5PW12O40 catalyzed diastereoselective synthesis of β-amino ketones via three component Mannich-type reaction in water

Tetrahedron ◽

10.1016/j.tet.2010.06.052 ◽

2010 ◽

Vol 66 (34) ◽

pp. 6858-6863 ◽

Cited By ~ 27

Author(s):

Ezzat Rafiee ◽

Sara Eavani ◽

Fereshte Khajooei Nejad ◽

Mohammad Joshaghani

Keyword(s):

Type Reaction ◽

Intermolecular Rhodium-Catalyzed Carbometalation/Heck-Type Reaction in Water

Angewandte Chemie ◽

10.1002/ange.200602585 ◽

2006 ◽

Vol 118 (38) ◽

pp. 6484-6486 ◽

Cited By ~ 22

Author(s):

Takuya Kurahashi ◽

Hiroshi Shinokubo ◽

Atsuhiro Osuka

Keyword(s):

Type Reaction ◽

Mannich-Type Reaction in Water in the Presence of a Surfactant.

ChemInform ◽

10.1002/chin.200715070 ◽

2007 ◽

Vol 38 (15) ◽

Author(s):

Junji Itoh ◽

Kohei Fuchibe ◽

Takahiko Akiyama

Keyword(s):

Type Reaction ◽

ChemInform Abstract: Ring-Opening Aldol-Type Reaction of 2,2-Dialkoxycyclopropanecarboxylic Esters with Carbonyl Compounds. Part 3. The Diastereoselective Synthesis of 2,3,4-Trisubstituted γ-Lactones.

ChemInform ◽

10.1002/chin.199401185 ◽

2010 ◽

Vol 25 (1) ◽

pp. no-no

Author(s):

S. SHIMADA ◽

Y. HASHIMOTO ◽

K. SAIGO

Keyword(s):

Carbonyl Compounds ◽

Ring Opening ◽

One-Pot Mannich-Type Reaction in Water

Category 1, Organometallics ◽

10.1055/sos-sd-007-00350 ◽

2004 ◽

pp. 1

Author(s):

T.-P. Loh

Keyword(s):

One Pot ◽

Type Reaction ◽

One-pot Mannich-Type Reaction In Water: HBF4 Catalyzed Condensation of Aldehydes, Amines, and Silyl Enolates for the Synthesis of β-Amino Carbonyl Compounds

Synlett ◽

10.1055/s-1999-2872 ◽

1999 ◽

Vol 1999 (9) ◽

pp. 1426-1428 ◽

Cited By ~ 53

Author(s):

Takahiko Akiyama ◽

Jun Takaya ◽

Hirotaka Kagoshima

Keyword(s):

Carbonyl Compounds ◽

One Pot ◽

Type Reaction ◽

Mannich-Type Reaction in Water in the Presence of a Surfactant

Synthesis ◽

10.1055/s-2006-950344 ◽

2006 ◽

Vol 2006 (23) ◽

pp. 4075-4080 ◽

Cited By ~ 1

Author(s):

Takahiko Akiyama ◽

Junji Itoh ◽

Kohei Fuchibe

Keyword(s):

Type Reaction ◽

Diastereoselective Synthesis of γ-Lactones by the Aldol-Type Reaction of Ethyl 2,2-Dialkoxycyclopropanecarboxylates with Aldehydes

Chemistry Letters ◽

10.1246/cl.1989.1293 ◽

1989 ◽

Vol 18 (7) ◽

pp. 1293-1296 ◽

Cited By ~ 8

Author(s):

Kazuhiko Saigo ◽

Shigeru Shimada ◽

Yukihiko Hashimoto ◽

Masaki Hasegawa

Keyword(s):

ChemInform Abstract: Ce(SO4)2-Catalyzed the Highly Diastereoselective Synthesis of Tetrahydroquinolines via an Imino Diels-Alder ABB′ Type Reaction and Their in vivo Toxicity and Imaging in Zebrafish Embryos.

ChemInform ◽

10.1002/chin.201635126 ◽

2016 ◽

Vol 47 (35) ◽

Author(s):

Carlos A. Martinez Bonilla ◽

Carlos E. Puerto Galvis ◽

Leonor Y. Vargas Mendez ◽

Vladimir V. Kouznetsov

Keyword(s):

Diels Alder ◽

Zebrafish Embryos ◽

In Vivo Toxicity ◽

ChemInform Abstract: Diastereoselective Synthesis of syn-β-Lactams Using Rh-Catalyzed Reductive Mannich-Type Reaction of α,β-Unsaturated Esters.

ChemInform ◽

10.1002/chin.201604094 ◽

2016 ◽

Vol 47 (4) ◽

pp. no-no

Author(s):

Motoyuki Isoda ◽

Kazuyuki Sato ◽

Masato Funakoshi ◽

Keiko Omura ◽

Atsushi Tarui ◽

...

Keyword(s):

Unsaturated Esters ◽