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(-)-(1R,3R,6S)-4-methylene-7,7-dimethylbicyclo[4.1.0]heptan-3-ol is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry: the 1, 3, and 6 positions are occupied by R (right), R, and S (left) configurations, respectively. The compound features a bicyclo[4.1.0]heptane ring system, which consists of two carbon rings fused together in a way that one of the rings is a three-membered ring. Additionally, it has a 4-methylene group, which is a methylene (CH2) group located at the 4-position, and a 3-hydroxyl group, indicating the presence of an alcohol functional group. The molecule also contains two methyl groups at the 7-position, contributing to its overall structure and properties. (-)-(1R,3R,6S)-4-methylene-7,7-dimethylbicyclo[4.1.0]heptan-3-ol is of interest in organic chemistry and may have applications in the synthesis of various pharmaceuticals and natural products due to its specific stereochemistry and functional groups.

4017-83-8

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4017-83-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4017-83-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4017-83:
(6*4)+(5*0)+(4*1)+(3*7)+(2*8)+(1*3)=68
68 % 10 = 8
So 4017-83-8 is a valid CAS Registry Number.

4017-83-8Relevant academic research and scientific papers

Stereoselective Synthesis of Carane-Type Hydroxythiols and Disulfides Based on Them

Banina,Sudarikov,Slepukhin,Frolova,Kuchin

, p. 240 - 247 (2016/07/06)

Isomeric 10-sulfanylcaran-4-ols and 4-sulfanylcaran-3-ols were synthesized and used to prepare disulfides in high yields.

Stereoselective synthesis of carane-based aminodiols as chiral ligands for the catalytic addition of diethylzinc to aldehydes

Szakonyi, Zsolt,Csillag, Kinga,Fueloep, Ferenc

, p. 1021 - 1027 (2011/09/20)

Key intermediate epoxy alcohol 4 was prepared regio- and stereoselectively from (+)-3-carene 1 via carene oxide 2 and (-)-trans-allyl alcohol 3. The lithium perchlorate-catalysed ring opening of 4 with secondary and primary achiral and chiral amines resulted in primary, secondary and tertiary aminodiols. Aminodiols 5-14 were applied as chiral catalysts in the enantioselective addition of diethylzinc to benzaldehyde, resulting in (R)- and (S)-1-phenyl-1-propanol with moderate enantioselectivity. N-Benzyl, N-methyl, and (S)- and (R)-N-methylbenzyl derivatives 7 and 10-13 were transformed into 1,3-oxazines 17-21 via highly regioselective ring closures. When 17-21 were applied as chiral catalysts in the addition of diethylzinc to aromatic and aliphatic aldehydes, high chiral induction in the tricyclic catalysts was observed. The effects of the substituents on the nitrogen of the aminodiols and 1,3-oxazines were studied in detail; the best enantioselectivity was observed in the case of N-methylbenzyl-substituted oxazine 19.

Synthesis of chiral thienylpyridines from naturally occurring monoterpenes: Useful ligands for cyclometallated complexes

Gianini, Michel,Von Zelewsky, Alex

, p. 702 - 706 (2007/10/03)

On treatment with ammonium acetate, α,β-unsaturated ketones or aldehydes can easily undergo condensation with acetylpyridinium salts (Krohnke reaction). Four 'thienylpyridine' ligands, derived from (-)-β-pinene, (+)-camphor, (+)-3-carene and (+)-2-carene, were prepared according to this method. The multistep syntheses to get (1R,5R)-3-methylenenopinone (5), (+)-3-methylenecamphor (10), (-)-3-caren-10-al (15) and (1S,6R)-7,7-dimethyl-3-methylenebicyclo[4.1.0]heptan-2-one (18) are also described.

Regioselective Routes to Nucleophilic Optically Active 2- and 3-Carene Systems

Paquette, Leo A.,Ross, Robert J.,Shi, Yao-Jun

, p. 1589 - 1598 (2007/10/02)

Commercially available (+)-3-carene (4) is shown to be capable of efficient conversion to vinyl bromides 28, 46, and 49 and to vinyl stannane 44.All four compounds stem from (+)-3-norcaranone (23), an optically pure ketone best prepared by epoxidation of 4, followed by oxirane ring opening, acetylation, ozonolysis, and CrCl2-promoted reduction.The strong proclivity exhibited by 23 to enolize in the cyclopropyl carbinyl sense is used to advantage to gain entry to 28 and 44.Remarkably, the tosylhydrazone of (+)-3-norcaranone (45) is distinguished from its ketoneprogenitor 23 by its capacity for highly regioselective deprotonation from the alternative α-position.The crossover has made possible synthetic access to 46 and 49.Other chemistry of this class of compounds is also presented, inluding a route to 51, a vinyl bromide epimeric to 49.Especially relevant to future work in the ingenol area is the ability of these molecules to serve as nucleophiles.Several reactions involving 28 are provided as exemplary of this property.

Acid-catalysed Terpenylations of Olivetol in the Synthesis of Cannabinoids

Crombie, Leslie,Crombie, W. Mary L.,Jamieson, Sally V.,Palmer, Christopher J.

, p. 1243 - 1250 (2007/10/02)

Examination of the toluene-p-sulphonic acid-catalysed reaction of (1S,2S,3R,6R)-(+)-trans-car-2-ene epoxide with olivetol shows that, inconsistently with the accepted mechanism, (3R,4R)-(-)-o- and -p-cannabidiols are produced as well as (3R,4R)-(-)-Δ1- and Δ6-tetrahydrocannabinols.Evidence is now presented that, as in Petrzilka's reaction employing chiral p-mentha-2,8-dien-1-ols, the reacting species is the delocalised (4R)-p-mentha-2,8-dien-1-yl cation (9).Similar terpenylation using (1S,3S,4R,6R)-(+)-trans-car-3-ene epoxide shows that besides the reported (-)-Δ6-THC, o- and p-cannabidiols, Δ1-THC and Δ4,8-iso-THC can also be produced.The nature of the products, the chirality, and the characteristics of the reaction implicate again the delocalised cation (9).Its formation via Kropp-type rearrangement is excluded and a pathway leading to (4R)-p-mentha-2,6,8-triene, which on protonation gives (9), is proposed.Protonated on C-8, the triene can be trapped and isolated as (4R)-p-mentha-2,6-dien-8-ol.The latter, made in (+/-)-form from citral, proved to be an excellent terpenylating agent for producing cannabinoids.Terpenylation of olivetol by the pinanes (1S,4S,5S)-(-)-cis-verbenol and (1R,5S,7R)-(+)-cis-chrysanthenol is compared.A major drawback of the latter is partial racemisation which occurs in the verbenone-chrysanthenone isomerisation during its photochemical preparation.Whilst Δ1-THC cannot be directly obtained from verbenol, its tertiary allylic cation permits a much higher yielding terpenylation than the secondary cation from chrysanthenol.

Formation of 1,2-Dioxolanes from Cyclopropanes

Ruecker, Gerhard,Frey, Klaus

, p. 389 - 392 (2007/10/02)

The already known carenols 5 and 7 are obtained by stereoselective oxirane cleavage of (1S,3S,4R,6R)-(+)-3α,4α-epoxycarane (4).Autoxidation of the ketone 8, derived from 7, failed to give any 1,2-dioxolane derivatives. 5 is converted to the hydroperoxide

Studies on the Terpenoids and Related Alicyclic Compounds. XXXII. A Synthesis of Chiral Dimethylcyclopropane Derivatives, Versatile Chiral Synthons for Casbane, Lathyrane, and Ingenane-Type Diterpenoids, from (+)-3-Carene

Satoh, Tsuyoshi,Okuda, Teruyoshi,Kaneko, Youhei,Yamakawa, Koji

, p. 1401 - 1410 (2007/10/02)

A synthesis of chiral dimethylcyclopropane derivatives, useful for the synthesis of casbane, lathyrane, and ingenane-type diterpenoids, from easily available (+)-3-carene is described.The silyl enol ether (8) was derived from (-)-cis-4-caranone (7b), which was obtained from (+)-3-carene (6).Ozonolysis of 8 gave 9a and 10.The right half segment (11b) for a synthesis of crotonitenone (3) was formed from 9a in three steps.The epoxide (12) was isomerized to a mixture of the allylic alcohols (13a) and (14a), which was transformed to the ketone (20) in five steps.Methylation of 20 followed by phosphorylation and reduction gave (+)-cis-4-caranone (23) in about 40 percent overall yield from 12.The methylester (+)-(32b) and its enantiomer (-)-(34b) were synthesized from (+)-6.Ozonolysis of a mixture of the silyl enol ether (30) and (31) followed by methylation with diazomethane gave 32a, which was hydrolyzed to give the desired (+)-32b.The enantiomer (-)-34b was derived from 32a in five steps.

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