ChemInform Abstract: OPTICALLY ACTIVE CARBODIIMIDES. PART II. DIASTEREOSELECTIVE SYNTHESIS OF 4-IMINO-2-AZETIDINONES

Z. KRAWCZYK; C. BELZECKI

doi:10.1002/chin.197942209

ChemInform Abstract: OPTICALLY ACTIVE CARBODIIMIDES. PART II. DIASTEREOSELECTIVE SYNTHESIS OF 4-IMINO-2-AZETIDINONES

Chemischer Informationsdienst ◽

10.1002/chin.197942209 ◽

1979 ◽

Vol 10 (42) ◽

Author(s):

Z. KRAWCZYK ◽

C. BELZECKI

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis

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Diastereoselective Synthesis of Novel Optically Active Five Membered O- and N-heterocyclic Compounds

Letters in Organic Chemistry ◽

10.2174/157017812800221744 ◽

2012 ◽

Vol 9 (2) ◽

pp. 81-88 ◽

Cited By ~ 1

Author(s):

Ervin Kovacs ◽

Ferenc Farkas ◽

Angelika Thurner ◽

Aron Szollosy ◽

Ferenc Faigl

Keyword(s):

Heterocyclic Compounds ◽

Optically Active ◽

Diastereoselective Synthesis

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ChemInform Abstract: Diastereoselective Synthesis of Optically Active Pyrrolizidine and Indolizidine Ring Systems Through Intramolecular Ene Reaction.

ChemInform ◽

10.1002/chin.199125250 ◽

2010 ◽

Vol 22 (25) ◽

pp. no-no

Author(s):

S. DIKE ◽

M. MAHALINGAM ◽

A. KUMAR

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis ◽

Ring Systems ◽

Ene Reaction

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Diastereoselective Synthesis of Optically Active C2-Substituted Spiro(4.5)decanes: Two Key Intermediates for Spirovetivane Sesquiterpenes.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.45.459 ◽

1997 ◽

Vol 45 (3) ◽

pp. 459-463 ◽

Cited By ~ 5

Author(s):

Yoshiji TAKEMOTO ◽

Taiichi OHRA ◽

Yasuhiro YONETOKU ◽

Chuzo IWATA

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis

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Diastereoselective synthesis of 3-[2-((N,N-dimethylamino)methyl)ferrocenyl]-4-(4-methoxyphenyl)hexan-3-ols, in racemic and optically active series, x-ray determination of their relative configuration

Organometallics ◽

10.1021/om00013a032 ◽

1994 ◽

Vol 13 (1) ◽

pp. 200-207 ◽

Cited By ~ 8

Author(s):

M. Gruselle ◽

B. Malezieux ◽

L. L. Troitskaya ◽

V. I. Sokolov ◽

L. M. Epstein ◽

...

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis ◽

Relative Configuration ◽

X Ray

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Diastereoselective synthesis of optically active (2 R ,5 R )-hexanediol

Applied Microbiology and Biotechnology ◽

10.1007/s00253-002-0936-5 ◽

2002 ◽

Vol 58 (5) ◽

pp. 595-599 ◽

Cited By ~ 39

Author(s):

J. Haberland, A. Kriegesmann, E. Wolfr

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis

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Regio and stereospecific ring expansion of optically active cyclopropylvinylcarbinols. Diastereoselective synthesis of cis Quercus- lactone b.

Tetrahedron Letters ◽

10.1016/s0040-4039(00)80345-7 ◽

1988 ◽

Vol 29 (13) ◽

pp. 1537-1540 ◽

Cited By ~ 15

Author(s):

Jacques Salaun ◽

Belkacem Karkour

Keyword(s):

Ring Expansion ◽

Optically Active ◽

Diastereoselective Synthesis

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ChemInform Abstract: Highly Diastereoselective Synthesis and Easy Method for Synthesis of Optically Active Sulfinate Esters from Aromatic Disulfides.

ChemInform ◽

10.1002/chin.200107084 ◽

2010 ◽

Vol 32 (7) ◽

pp. no-no

Author(s):

Abdol Reza Hajipour ◽

Fereshteh Islami

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis ◽

Easy Method ◽

Sulfinate Esters

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ChemInform Abstract: Reactions of Complex Ligands. Part 43. Optically Active Aminocarbene Complexes: Reagents for the Regiospecific and Diastereoselective Synthesis of γ-Lactams.

ChemInform ◽

10.1002/chin.199137221 ◽

2010 ◽

Vol 22 (37) ◽

pp. no-no

Author(s):

K. H. DOETZ ◽

R. WEBER

Keyword(s):

Optically Active ◽

Diastereoselective Synthesis

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ChemInform Abstract: Regio- and Stereospecific Ring Expansion of Optically Active Cyclopropylvinylcarbinols (VI). Diastereoselective Synthesis of cis-Quercus Lactone b (VIIIa).

ChemInform ◽

10.1002/chin.198834152 ◽

1988 ◽

Vol 19 (34) ◽

Author(s):

J. SALAUEN ◽

B. KARKOUR

Keyword(s):

Ring Expansion ◽

Optically Active ◽

Diastereoselective Synthesis

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Diastereoselective alkoxymethylation of aromatic aldehydes with chiral lithiomethyl ethers. Synthesis of optically active monoprotected glycols

Canadian Journal of Chemistry ◽

10.1139/v98-193 ◽

1998 ◽

Vol 76 (10) ◽

pp. 1338-1343 ◽

Cited By ~ 2

Author(s):

Viviana L Ponzo ◽

Teodoro S Kaufman

Keyword(s):

Key Words ◽

Aromatic Aldehydes ◽

Optically Active ◽

Asymmetric Induction ◽

Diastereoselective Synthesis ◽

Benzyl Alcohols

The synthesis of optically active α-alkoxymethyl benzyl alcohols by reaction of polysubstituted benzaldehydes with chiral α-alkoxymethyllithiums, easily obtained by transmetallation of the corresponding α-alkoxystannanes with n-butyllithium, is reported. Chemical yields of the transformation are good while low asymmetric induction (<1.6:1) is obtained. Key words: diastereoselective synthesis, monoprotected glycols, chiral alkoxymethyllithiums, addition to aldehydes, optically active alcohols.

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