Fortschritte Der Chemischen Forschung
DOI: 10.1007/bfb0051797
|View full text |Cite
|
Sign up to set email alerts
|

Chlorophyll

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
6
0

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 30 publications
(6 citation statements)
references
References 365 publications
0
6
0
Order By: Relevance
“…Cambie et al18 have isolated cyclopheophorbide and determined its structure by X-ray diffraction. It is worth noting, that the structure of naturally occurring cyclopheophorbide, which was first isolated in 1986, is identical to that of the cyclopheophorbide prepared from chlorophyll a (4) by partial synthesis (see Scheme 12) in Eschenmoser's laboratory19 some years before. Structural elucidation of chlorophyllone a (11), an oxidation product of 10, was achieved by classical spectroscopic methods.20 Both compounds exhibit antioxidative properties and protect the animals containing the chlorin derivatives 10 and 11 against unwanted oxidation processes.…”
Section: Chlorinsmentioning
confidence: 88%
See 4 more Smart Citations
“…Cambie et al18 have isolated cyclopheophorbide and determined its structure by X-ray diffraction. It is worth noting, that the structure of naturally occurring cyclopheophorbide, which was first isolated in 1986, is identical to that of the cyclopheophorbide prepared from chlorophyll a (4) by partial synthesis (see Scheme 12) in Eschenmoser's laboratory19 some years before. Structural elucidation of chlorophyllone a (11), an oxidation product of 10, was achieved by classical spectroscopic methods.20 Both compounds exhibit antioxidative properties and protect the animals containing the chlorin derivatives 10 and 11 against unwanted oxidation processes.…”
Section: Chlorinsmentioning
confidence: 88%
“…and D of Bonellin ( 12)* 75 C0'CH= 0 (a) Lawesson's reagent, THF, reflux, 30 min. (b) HC(OMe)3, TsOH, benzene, reflux, 2.5 h. (c) (1) O3/O2, MeOH, CH2CI2, -80 °C; (2) Me2S, room temperature, 3 h; (3) HC(OMe>3, TsOH, room temperature, 12 h. (d) (1) Raney-Ni, H2, MeOH, room temperature, 4.5 h; (2) HCIO4 (60%), MeCN/H20, room temperature, 2.5 h; (3) NH3/NH4CI, MeOH, room temperature, 4.5 h; (4) AcOH, reflux, 5.5…”
Section: Total Synthesis Of Naturally Occurring Chlorinsmentioning
confidence: 99%
See 3 more Smart Citations